Portable penile erection bionic treatment system and method
The portable penile erection bionic treatment system, which combines negative pressure, heating, fluid injection, and massage, solves the problems of high cost, high risk, and insignificant effect of existing treatment methods, and achieves effective treatment during sexual life and builds patient confidence.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2023-01-19
- Publication Date
- 2026-04-10
AI Technical Summary
Existing treatments for erectile dysfunction are expensive, have high surgical risks, are not very effective, and are not suitable for sexual use. Furthermore, traditional negative pressure erection devices can negatively impact penile recovery.
This invention provides a portable bionic treatment system for penile erection that combines negative pressure, heating, fluid injection, and massage. Through a treatment sleeve made of flexible material and multiple sensors and electrodes, it monitors and adjusts treatment parameters in real time to achieve comprehensive treatment.
This system can be used during sexual intercourse to prolong erection time, improve treatment effectiveness, enhance patient confidence, has a simple and portable structure, is highly comfortable, provides accurate detection, and offers multi-point treatment to meet different needs.
Smart Images

Figure CN121818210A_ABST
Abstract
Description
Technical Field
[0001] This invention relates to the field of medical devices and supplies, and more particularly to a portable penile erection bionic treatment system and method. Background Technology
[0002] Erectile dysfunction (ED) is a common sexual dysfunction. Currently, Traditional Chinese Medicine (TCM) treatment for ED focuses on warming and tonifying kidney yang. While TCM can alleviate some symptoms, it cannot cure the condition and can leave many problems for patients, even causing psychological burden. Another widely used method for treating ED includes implants, which are essentially internal prostheses that require surgical insertion into the penis. However, these surgical implants are usually expensive and not always effective. Another method involves placing a plastic cylinder outside the penis and using a vacuum pump to restrict venous blood flow. The corpora cavernosa fill with the trapped blood, thus creating an erection. While this method does not affect urination or the ability to achieve orgasm, the surgery requiring such implants can cause pain, infection, or scarring. Furthermore, the effect is short-lived, and prolonged use may cause penile damage such as necrosis. Most importantly, it is unsuitable for use during sexual intercourse, hindering the patient's psychological confidence.
[0003] Therefore, negative pressure erection therapy is currently one of the clinical treatment methods for erectile dysfunction. While simple in structure, it affects the clinical effectiveness of penile rehabilitation. There is an urgent need to improve existing devices to better meet the needs of patients. Summary of the Invention
[0004] One advantage of this invention is that it provides a portable penile erection bionic treatment system and method that can be used during sexual intercourse, and can adjust the corresponding treatment parameters in real time according to the situation to prolong the erection time and help patients build psychological confidence.
[0005] Another advantage of this invention is that it provides a portable penile erection bionic treatment system and method, in which multiple methods such as negative pressure, heating, fluid injection and massage can work synergistically to accelerate the engorgement of the corpora cavernosa, strengthen the corpora cavernosa, enhance the treatment effect and shorten the treatment time.
[0006] Another advantage of the present invention is that it provides a portable penile erection bionic treatment system and method. The system has a simple structure, small size, can be fixed to the patient's body, is easy to use, and can also be disassembled and placed separately for easy carrying.
[0007] Another advantage of the present invention is that it provides a portable penile erection bionic treatment system and method, wherein the massage strips arranged at intervals can provide support and massage the penis to promote penile erection.
[0008] Another advantage of this invention is that it provides a portable penile erection bionic treatment system and method, wherein the treatment sleeve is made of flexible material, which has good fit and wrapping properties for the penis, making it comfortable for the patient to use and providing a good experience. Moreover, it provides all-round wrapping, accurate data monitoring, and multiple treatment points, thus achieving better treatment results.
[0009] Another advantage of this invention is that it provides a portable penile erection bionic treatment system and method, in which pressure sensors and temperature sensors are arranged at multiple intervals, making the detection more accurate and ensuring that the entire penis is detected, so as to adjust the parameters more precisely and achieve better treatment results.
[0010] Another advantage of the present invention is that it provides a portable penile erection bionic treatment system and method, in which multiple massage strips and multiple electrodes are arranged alternately, which can be arranged longitudinally or in a ring, so as to wrap around the outside of the penis in all directions, providing multi-point treatment and improving the therapeutic effect.
[0011] According to one aspect of the present invention, a portable penile erection bionic treatment system is provided, comprising:
[0012] A treatment unit includes a treatment sleeve and at least one extension connected to the rear end of the treatment sleeve. The treatment sleeve includes an inner shell, an outer shell, and a plurality of connectors. The connectors are connected between the inner shell and the outer shell, dividing the inner shell and the outer shell into a plurality of independent and closed connecting cavities and a plurality of negative pressure cavities. The treatment sleeve also has a fitting cavity, and the inner shell forms the outer wall of the fitting cavity for fitting onto the outside of the patient's penis.
[0013] A portable unit, the portable unit including a portable body and a fitting surface, the fitting surface forming one side of the portable body to fit the patient's waist;
[0014] A monitoring unit, installed inside the treatment sleeve, is used to monitor the temperature, pressure, rigidity, and duration of the penile surface; and
[0015] A control unit is mounted on the portable body and connected to the treatment unit and the monitoring unit via the extension to send treatment commands.
[0016] The control unit includes a processor and a control panel, a vacuum pump, a motor, and a recording module connected to the processor. The portable unit also includes a liquid storage tank and a connecting pipe connected to the liquid storage tank. The control panel is disposed on the surface of the portable body, and the vacuum pump, the motor, the processor, the recording module, the liquid storage tank, and the connecting pipe are all disposed inside the portable body.
[0017] According to an embodiment of the present invention, the portable unit has a negative pressure interface, a motor interface, and a connecting pipe interface, which are respectively connected to the vacuum pump, the motor, and the connecting pipe. The rear end of the extension section is provided with a negative pressure connection end, a motor connection end, and a pipe connection end, which are detachably connected to the negative pressure interface, the motor interface, and the connecting pipe interface, respectively. The front end of the extension section is integrally formed with the treatment sleeve. A negative pressure pipe is also provided inside the extension section, which communicates between the negative pressure connection end and the negative pressure chamber. The liquid storage tank is connected to the negative pressure chamber through the connecting pipe, the pipe connection end, and the extension section. The extension section also includes a pressure relief valve, which is provided at the rear end of the extension section and is connected to the negative pressure pipe.
[0018] According to another embodiment of the present invention, the rear end of the extension section is integrally formed with the portable body, and the front end of the extension section is detachably connected to the treatment sleeve. The front end of the extension section is provided with a negative pressure connection end, a motor connection end, and a tube connection end, which are respectively connected to the vacuum pump, the motor, and the connecting tube. The treatment unit has a negative pressure interface, a motor interface, and a connecting tube interface, which are respectively disposed adjacent to each other at the rear end of the treatment sleeve and are respectively detachably connected to the negative pressure interface, the motor interface, and the connecting tube interface. The negative pressure interface and the connecting tube interface are both connected to the negative pressure chamber. The motor interface is electrically connected to the monitoring unit. The portable unit also includes a pressure relief valve, which is disposed on the portable body and connected to the negative pressure tube.
[0019] The monitoring unit includes at least one temperature sensor, at least one pressure sensor, at least one massage strip, and at least one electrode. The temperature sensor and the pressure sensor are respectively installed in the connecting cavity. The massage strip and the electrode are installed alternately on the outer wall of the inner housing. The monitoring unit is connected to the control unit through the extension section, receives instructions from the control unit, and performs corresponding operations.
[0020] The treatment sleeve also has an interface and an opening, the interface and the opening being respectively located at the rear and front ends of the treatment sleeve and communicating with the sleeve cavity. The treatment sleeve is made of a flexible elastic material. The portable unit also includes a power supply unit, which is located in the portable body and electrically connected to the control unit. The control unit also includes a voice control unit, which is connected to the processor. The voice control unit includes a prompter, a microphone, and an alarm, all of which are located in the portable body to establish communication between the operator and the processor.
[0021] According to one embodiment of the present invention, the massage strip and the electrode are both strip-shaped, longitudinally arranged inside the treatment sleeve, and electrically connected to the motor and the processor, and the plurality of negative pressure chambers are longitudinally arranged in the treatment sleeve.
[0022] According to another embodiment of the present invention, the massage strip and the electrode are both strip-shaped and are arranged in an annular manner inside the treatment sleeve. The negative pressure chamber includes two longitudinal negative pressure chambers and a plurality of annular negative pressure chambers. One of the longitudinal negative pressure chambers is connected to the vacuum pump through the extension section, and the other longitudinal negative pressure chamber is connected to the liquid storage tank through the extension section. The annular negative pressure chamber surrounds the treatment sleeve and communicates with the longitudinal negative pressure chambers.
[0023] According to another aspect of the present invention, the present invention also provides a method of operating a portable penile erection bionic treatment system, comprising the following steps:
[0024] (A) A portable unit is fixed to the patient's waist by attaching a treatment sleeve to the outside of the patient's penis, and the treatment sleeve is connected to the portable unit;
[0025] (B) Operate a control panel and start a control unit according to the preset treatment temperature, treatment pressure and vibration frequency. The control unit sends a command to a monitoring unit, which is located inside the treatment sleeve.
[0026] (C) The treatment sleeve and the monitoring unit enter the working mode according to the instructions. The monitoring unit monitors the temperature, pressure, erection hardness, and duration of the patient's penis in real time and provides feedback to the control unit and the patient; and
[0027] (D) The control unit adjusts itself based on the data fed back by the monitoring unit to adapt to the different needs of different patients.
[0028] The operating method further includes a step (E): after treatment, the portable penile erection bionic treatment system is turned off, and the pressure of a negative pressure tube and at least one negative pressure chamber included in the treatment unit is released through a pressure relief valve. The treatment sleeve is then removed. In the above steps, the monitoring unit includes at least one pressure sensor, at least one temperature sensor, at least one massage strip, and at least one electrode, all of which are disposed on the treatment sleeve. The treatment sleeve also has at least one negative pressure chamber connected to a vacuum pump of the control unit to achieve negative pressure and fluid injection. The treatment sleeve is made of a flexible material, wraps around and fits the outside of the patient's penis, and changes with the changes in the penis. Attached Figure Description
[0029] Figure 1This is a schematic diagram of a portable penile erection bionic treatment system according to a preferred embodiment of the present invention.
[0030] Figure 2 This is an exploded view of the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0031] Figure 3 This is a schematic diagram of the portable unit included in the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0032] Figure 4 This is a schematic diagram of the control unit included in the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0033] Figure 5 This is a partial structural diagram of the treatment sleeve included in the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0034] Figure 6A and Figure 6B This is a cross-sectional schematic diagram of the treatment sleeve included in the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0035] Figure 6C This is a flowchart illustrating the operation of the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0036] Figure 7A and Figure 7B This is a schematic diagram of a modified embodiment of the treatment sleeve included in the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0037] Figure 7C This is a flowchart illustrating a modified embodiment of the portable penile erection bionic treatment system according to the above-described preferred embodiment of the present invention.
[0038] Figure 8 This is a schematic diagram of the structure of the portable penile erection bionic treatment system according to another preferred embodiment of the present invention. Detailed Implementation
[0039] The following description is intended to disclose the present invention and enable those skilled in the art to implement it. The preferred embodiments described below are merely examples, and other obvious variations will occur to those skilled in the art. The basic principles of the invention defined in the following description can be applied to other embodiments, modifications, improvements, equivalents, and other technical solutions that do not depart from the spirit and scope of the invention.
[0040] Those skilled in the art should understand that, in the disclosure of this invention, the terms "longitudinal," "annular," "upper," "lower," "front," "rear," "top," "bottom," "inner," and "outer," etc., indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are only for the convenience of describing this invention and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, the above terms should not be construed as limiting this invention.
[0041] It is understood that the term "a" should be understood as "at least one" or "one or more", that is, in one embodiment, the number of an element can be one, while in another embodiment, the number of the element can be multiple, and the term "a" should not be understood as a limitation on the number.
[0042] Reference Appendix Figure 1 To be continued Figure 6C As shown, a portable penile erection bionic treatment system according to a preferred embodiment of the present invention is illustrated. In this preferred embodiment, the portable penile erection bionic treatment system includes a treatment unit 10, a control unit 20, a monitoring unit 30, and a portable unit 40. The control unit 20 is disposed within the portable unit 40, and the monitoring unit 30 is disposed inside the treatment unit 10. Both the treatment unit 10 and the monitoring unit 30 are connected to the control unit 20. Under the control of the control unit 20, the monitoring unit 30 is adjusted to enable the treatment unit 10 to achieve the corresponding therapeutic effect. The portable unit 40 is adapted for detachable connection to the human body, so that the portable penile erection bionic treatment system can be used in conjunction with sexual intercourse.
[0043] In this embodiment, the detachable connection between the treatment unit 10 and the portable unit 40 facilitates carrying and storage, and can be installed simply for use. This detachable connection also allows the user to easily attach the treatment unit 10 to the outside of the penis, fix the portable unit 40 to the waist, and then connect the two. It is convenient to use and easy to disassemble after use. Furthermore, the portable unit 40 can be used continuously; only the treatment unit 10 needs to be replaced to achieve continuous treatment.
[0044] The treatment unit 10 includes a treatment sleeve 11 and at least one extension 12, the extension 12 being connected to the rear end of the treatment sleeve 11. In this embodiment, the extension 12 is integrally formed into the treatment sleeve 11 and extends outward from the rear end side of the treatment sleeve 11. In other embodiments of the present invention, the extension 12 and the treatment sleeve 11 may be detachably connected. The extension 12 may be one, or two or three spaced apart, and its number is not limited by this embodiment.
[0045] In this invention, the direction in which the treatment sleeve 11 is applied to the tip of the penis is considered forward, and the direction in which the treatment sleeve 11 faces the waist of the human body is considered backward.
[0046] The treatment sleeve 11 has a connecting cavity 1100, a connecting interface 1101, and an opening 1102. Both the connecting interface 1101 and the opening 1102 are connected to the connecting cavity 1100. The connecting interface 1101 is located at the rear end of the treatment sleeve 11, and the opening 1102 is located at the front end. The extension section 12 is located on one side of the rear end of the treatment sleeve 11 and does not obstruct the connecting interface 1101. The treatment sleeve 11 is fitted to the human penis. Therefore, when the treatment sleeve 11 is used, the penis enters the connecting cavity 1100 through the connecting interface 1101. At this time, the opening 1102 is located at the front end of the penis, allowing the penis to communicate with the outside and ensuring normal ejaculation, thus enabling its use during sexual intercourse.
[0047] The treatment sleeve 11 has a predetermined elasticity, so the size of the sleeve cavity 1100, the sleeve interface 1101 and the opening 1102 can be changed to accommodate different people.
[0048] The treatment sleeve 11 includes an inner shell 111, an outer shell 112, and a plurality of connectors 113. The connectors 113 are connected between the inner shell 111 and the outer shell 112, thereby dividing the inner shell 111 and the outer shell 112 into a plurality of connecting cavities 1103 and a plurality of negative pressure cavities 1104, so as to facilitate the installation of different treatment components and the formation of a negative pressure environment for negative pressure treatment.
[0049] The socket 1100 is disposed inside the inner shell 111, and the inner wall of the inner shell 111 forms the external structure of the socket 1100. The inner wall of the inner shell 111 is smooth and soft, suitable for conforming to the outside of the penis, providing greater comfort to the user.
[0050] The inner shell 111 and the outer shell 112 are connected at both ends, so that the multiple connecting cavities 1103 and the multiple negative pressure cavities 1104 form multiple independent and closed cavities. The connecting cavity 1103 is located between the inner shell 111 and the outer shell 112. After the components are installed, it can still be used normally during sexual intercourse without causing any damage to the penis.
[0051] The treatment sleeve 11 is made of a flexible material with predetermined elasticity, allowing it to deform appropriately with the curvature and erection of the penis to meet the needs of treatment and sexual intercourse. Furthermore, the flexible treatment sleeve 11 fits snugly against the outside of the patient's penis, providing good coverage, facilitating treatment, and preventing it from easily slipping off. Especially after negative pressure is applied and the penis is erect, it adapts to changes in penis size, maintaining a good fit throughout the entire process.
[0052] The extension section 12 extends from the rear end of the treatment sleeve 11 to the portable unit 40, so that the portable unit 40 is connected to the treatment sleeve 11 through the extension section 12, forming an integrated portable penile erection bionic treatment system. The extension section 12 is also made of flexible material to prevent hard materials from scratching the human body during application.
[0053] The portable unit 40 includes a portable body 41 and two connecting straps 42. The connecting straps 42 are respectively connected to both sides of the portable body 41. The portable body 41 is ergonomically designed to conform to the curve of the human waist to fit snugly. The connecting straps 42 are suitable for binding around the waist to make the portable body 41 fit the human body more closely and prevent it from slipping off during use. Therefore, the connecting straps 42 can be implemented as a detachable connection structure such as buckles or Velcro, which can not only fix it to the patient's waist, but also adjust the size of the two connecting straps after connection to accommodate people of different body types.
[0054] Since the portable unit 40 can be strapped to a person's waist, when the treatment sleeve 10 is fitted over the penis, the portable unit 40 is securely positioned at the waist. Therefore, the portable penile erection bionic treatment system of the present invention is suitable for use during sexual intercourse, achieving therapeutic purposes, relieving psychological stress, and building self-confidence in the patient.
[0055] The portable unit 40 has a mounting cavity 400 and a fitting surface 43. The fitting surface 43 is disposed on the back of the portable body 41, forming a side portion of the portable body 41. The fitting surface 43 is ergonomically designed and positioned to fit the skin of the waist. In this embodiment, it adopts an arc-shaped design to closely fit the patient's waist and is made of a soft material for greater comfort. The mounting cavity 400 is disposed inside the portable body 41 to facilitate the installation of the control unit 20 and to facilitate the adjustment of the control unit 20 to better meet treatment needs.
[0056] The portable unit 40 also has a negative pressure interface 44, a motor interface 45, and a connecting pipe interface 46, which are designed adjacent to each other to facilitate the detachable connection of the extension section 12. The negative pressure interface 44, the motor interface 45, and the connecting pipe interface 46 are all located on the surface of the portable body 41.
[0057] The portable unit 40 further includes a liquid reservoir 48 and a connecting pipe 49. The connecting pipe 49 connects the liquid reservoir 48 and the connecting pipe interface 46, allowing liquid inside the liquid reservoir 48 to enter the treatment unit 10 through the connecting pipe 49 and the connecting pipe interface 46. The liquid reservoir 48 is detachably disposed inside the portable body 41, thus the outer shell of the portable body 41 can be opened to facilitate inspection and replacement of the liquid reservoir 48 and the control unit 20 installed inside the mounting cavity 400, thereby extending the service life of the entire device.
[0058] The control unit 20 includes a control panel 21, a voice control unit 22, a vacuum pump 23, a motor 24, a processor 25, and a recording module 26. The control panel 21, the voice control unit 22, the vacuum pump 23, the motor 24, and the recording module 26 are all electrically connected to the processor 25, and the processor 25 is controlled by manipulating the control panel 21, thereby controlling each component.
[0059] The control panel 21 is located on the surface of the portable main body 41, featuring an LCD screen for easy human operation. Besides controlling the portable penile erection bionic treatment system via the control panel 21, the control unit 20 can also be connected wirelessly to mobile phones, tablets, computers, and other electronic devices via WiFi, Bluetooth, etc., allowing for control through these devices as well. Data can be set, stored, and displayed, enabling patients to view usage frequency, treatment data, and treatment effects at any time.
[0060] The voice control unit 22 includes a prompter 221, a microphone 222, and an alarm 223. The microphone 222 is suitable for the user to input corresponding commands via voice. The prompter 221 is used to prompt the input commands and the status of the penile erection bionic treatment system, allowing the patient to promptly understand the treatment status, rest status, and temperature, pressure, vibration frequency, and other conditions of the penile erection bionic treatment system during treatment. The alarm 223 is used to alert the patient to any abnormalities in the system.
[0061] The vacuum pump 23 is installed in the mounting cavity 400 and connected to the extension section 12 via the negative pressure interface 44. The extension section 12 includes a negative pressure tube 121 and a negative pressure connection end 122. The negative pressure connection end 122 is disposed at the end of the negative pressure tube 121, wherein the negative pressure connection end 122 is detachably mated with the negative pressure interface 44, so that the negative pressure tube 121 extends from the negative pressure interface 44 to the negative pressure cavity 1104, facilitating the formation of a negative pressure environment inside the treatment sleeve 10 through the vacuum pump 23 and the negative pressure tube 121 for negative pressure treatment to promote penile erection.
[0062] The extension section 12 further includes a pipe connection end 123 and a liquid inlet pipe embedded inside the extension section 12. In this embodiment, the liquid inlet pipe is implemented as a channel opened in the shell of the extension section 12, and the liquid inlet pipe can also be implemented as a pipeline. The liquid inlet pipe connects the negative pressure chamber 1104 and the pipe connection end 123. The pipe connection end 123 is disposed at the end of the extension section 12 and is detachably matched and connected to the connecting pipe interface 46. Through the connection between the pipe connection end 123 and the connecting pipe interface 46, the liquid storage tank 48 and the negative pressure chamber 1104 are connected. When the negative pressure chamber 1104 forms a negative pressure environment through the vacuum pump 23, the liquid in the storage tank 48 enters the negative pressure chamber 1104 under the action of negative pressure. The control unit 20 shuts off the negative pressure pump 23 according to the preset negative pressure time, so that the negative pressure chamber 1104 is filled with the liquid flowing out from the storage tank 48. The suction effect of negative pressure and the peristalsis of the liquid promote penile erection, so as to achieve a better treatment effect.
[0063] The extension section 12 further includes multiple wires embedded inside the housing of the extension section 12 and a motor connection terminal 124 connected to the wires. The motor connection terminal 124 is located at the end of the extension section 12, adjacent to the negative pressure connection terminal 122 and the pipe connection terminal 123. The motor connection terminal 124 is detachably electrically connected to the motor interface 45 to electrically connect the treatment unit 10 and the monitoring unit 30 to the control unit 20.
[0064] The extension section 12 also includes a pressure relief valve 125 and a liquid outlet 126, both of which are connected to the negative pressure tube 121. During application of the portable penile erection bionic treatment system, the pressure relief valve 125 remains sealed to create a negative pressure state inside the negative pressure tube 121 and the negative pressure chamber 1104, which is beneficial for penile erection. After treatment, when the portable penile erection bionic treatment system is turned off, the negative pressure tube 121 and the negative pressure chamber 1104 remain under negative pressure. At this time, opening the pressure relief valve 125 connects the negative pressure tube 121 to the outside, changing the pressure inside the negative pressure tube 121 and the negative pressure chamber 1104, facilitating the removal of the treatment sleeve 11. The liquid inside the negative pressure chamber 1104 is discharged through the liquid outlet 126.
[0065] The portable unit 40 also includes a power supply unit 47, which is replaceably mounted in the mounting cavity 400. The power supply unit 47 is connected to the circuit structure of the control unit 20 to supply power to the control unit 20, enabling the portable penile erection bionic treatment system to function normally. The power supply unit 47 can accommodate a rechargeable battery or dry cell battery, and the battery is replaceable. It does not require a direct power connection via a wire, thus making it more convenient to carry and use during sexual activity.
[0066] The monitoring unit 30 includes at least one temperature sensor 31, at least one pressure sensor 32, multiple massage strips 33, and multiple electrodes 34. The temperature sensor 31 and the pressure sensor 32 are spaced apart and disposed on the outer wall of the inner shell 111, located inside the connecting cavity 1103 between the inner shell 111 and the outer shell 112, for comprehensive monitoring of the temperature of the treatment sleeve 11. Because the inner shell 111 is thin and facilitates heat conduction, the temperature sensor 31 can monitor the temperature of the penis in real time, allowing the control unit 20 to adjust it promptly, bringing the penis temperature closer to the predetermined treatment temperature. The predetermined treatment temperature set in this invention is 36-37°C and can be adjusted in real time. This treatment temperature facilitates penile erection and prolongs the erection time.
[0067] The pressure sensor 32 can monitor the pressure of the penis in real time and adjust it promptly to ensure that the pressure of the treatment sleeve reaches the therapeutic level, promoting penile erection, satisfying the needs of sexual intercourse, and achieving the therapeutic goal. Furthermore, it can change the pressure parameters according to the hardness and duration of penile erection to prolong erection time and improve the treatment effect.
[0068] The massage strips 33 are spaced apart on the outer wall of the inner housing 111, and multiple massage strips 33 are longitudinally arranged spaced apart on the outer side of the inner housing 111. During application, they wrap around the penis, providing comprehensive massage to promote blood circulation and erection. The massage strips 33 are flexible, thin strips and are electrically connected to the motor 24 via wires. Under the control of the control panel 21 and the processor 25, the massage strips 33 vibrate to massage the penis, promoting blood circulation and achieving therapeutic effects while providing comfort.
[0069] The electrodes 34 are longitudinally arranged at intervals on the outer wall of the inner shell 111. The multiple electrodes 34 are located on the outside of the inner shell 111, so that they can wrap around the outside of the penis during use. The electrodes 34 are connected to the motor 24 through the wires to supply low-frequency current to the electrodes 34, so as to achieve the purpose of heating the penis in all directions.
[0070] It is worth mentioning that, in this embodiment, the massage strip 33 and the electrode 34 are both thin strips, arranged longitudinally on the outer wall of the inner shell 111, that is, along the length direction of the treatment sleeve 11, and their length is equivalent to the length of the treatment sleeve 11, so that the entire penis can be treated during the treatment process.
[0071] The recording module 26 is installed inside the portable body 41 and electrically connected to the monitoring unit 30 to record information from the temperature sensor 31, the pressure sensor 32, the massage strip 33, and the electrode 34. It collects the penile erection hardness, erection duration, and the number and time of parameter adjustments during each use, and stores the information for the patient to query. This allows for the redesign of treatment parameters based on the actual situation, adjustment of the treatment plan, and achievement of better treatment results.
[0072] Reference Appendix Figures 7A to 7C As shown, in another embodiment of the present invention, the treatment unit 10A is modified. In this embodiment, the treatment unit 10A includes a treatment sleeve 11A and an extension 12A connected to the rear end of the treatment sleeve 11A. The extension 12A is the same as in the above embodiment and will not be described again here.
[0073] The treatment sleeve 11A has a sleeve cavity 1100A inside. The rear end and front end of the treatment sleeve 11A are respectively provided with a sleeve interface 1101A and an opening 1102A. The sleeve interface 1101A and the opening 1102A are connected to the sleeve cavity 1100A to allow the penis to enter without affecting ejaculation, so as to be used in conjunction with sexual intercourse.
[0074] The treatment sleeve 11A includes an inner shell 111A, an outer shell 112A, and a plurality of connectors 113A. The connectors 113A are connected between the inner shell 111A and the outer shell 112A to divide the treatment sleeve 11A into a plurality of connecting cavities 1103A and a plurality of negative pressure cavities 1104A, all located between the inner shell 111A and the outer shell 112A, so as to facilitate the installation of the monitoring unit 30A, the formation of a negative pressure environment, and the injection of liquid.
[0075] The negative pressure chamber 1104A includes two longitudinal negative pressure chambers 11041A and multiple annular negative pressure chambers 11042A. The annular negative pressure chambers 11042A and the longitudinal negative pressure chambers 11041A are connected. One of the longitudinal negative pressure chambers 11041A is connected between the vacuum pump 23 and the annular negative pressure chamber 11042A via the extension section 12A, and the other longitudinal negative pressure chamber 11041A is connected between the liquid storage tank 48 and the annular negative pressure chamber 11042A via the extension section 12A. Under the action of the vacuum pump 23, a negative pressure environment is formed in the longitudinal negative pressure chambers 11041A and the annular negative pressure chambers 11042A. The liquid inside the liquid storage tank 48 enters the longitudinal negative pressure chambers 11041A and the annular negative pressure chambers 11042A under the negative pressure to promote penile erection.
[0076] The longitudinal negative pressure chamber 11041A is disposed inside the two sides of the treatment sleeve 11A, and the annular negative pressure chambers 11042A are disposed in a ring-shaped arrangement at intervals inside the treatment sleeve 11A, with both ends of the annular negative pressure chambers 11042A connected to the longitudinal negative pressure chambers 11041A. In application, a negative pressure environment can be formed around the entire penis, promoting better penile erection and helping to prolong erection time.
[0077] The monitoring unit 30A includes multiple temperature sensors 31A, multiple pressure sensors 32A, multiple massage strips 33A, and multiple electrodes 34A. The temperature sensors 31A and pressure sensors 32A are disposed on the outer side wall of the inner housing 111A and located within the connecting cavity 1103A. The massage strips 33A and electrodes 34A are both strip-shaped and arranged in a ring between the inner housing 111A and the outer housing 112A, surrounding the outer side wall of the inner housing 111A. The temperature sensors 31A and pressure sensors 32A are located in the middle of the massage strips 33A and electrodes 34A, allowing the components to be spaced apart.
[0078] The massage strips 33A and the electrodes 34A are arranged in a ring or dot pattern, spaced apart, on the outer wall of the inner shell 111A. This allows for comprehensive treatment of the entire penis, promoting blood circulation and removing blood stasis, thus achieving better therapeutic results.
[0079] Reference Appendix Figure 8 The present invention is shown in another preferred embodiment. In this embodiment, the portable unit 40B and the treatment unit 10B of the portable penile erection bionic treatment system are modified.
[0080] The treatment unit 10B includes a treatment sleeve 11B and an extension 12B, wherein the extension 12B and the treatment sleeve 11B are detachably connected. That is, the negative pressure connection end 122B, the motor connection end 123B and the tube connection end 124B in the above embodiment are disposed at the front end of the extension 12B, and the negative pressure interface, the motor interface and the connecting tube interface in the above embodiment are disposed at the rear end of the treatment sleeve 11B, namely the negative pressure interface 114B, the motor interface 115B and the connecting tube interface 116B, respectively, so that the treatment sleeve 11B can generate negative pressure, supply power and inject liquid. The working method is the same as in the above embodiment, and will not be described again here.
[0081] The portable unit 40B includes a portable body 41B and an adhesive surface 43B. The adhesive surface 43B has an arc-shaped structure and is located on one side of the portable body 41B. It is adhesive and can be detachably attached to the waist of the human body after the protective film is removed, and can be fixed to the human body without the need for a connecting strap.
[0082] The pressure relief valve 125B is located on the side of the portable body 41B to facilitate pressure relief after use. The liquid outlet 126B is still located on the extension section 12B to facilitate liquid discharge.
[0083] It is worth mentioning that in this embodiment, the rear end of the extension segment 12B is integrally formed with the portable main body 41B, and the front end of the extension segment 12B is detachably connected to the treatment sleeve 11B, which facilitates replacement and disassembly, making it convenient to use. When different patients or the same patient uses it multiple times, only the treatment sleeve 11B needs to be replaced, eliminating the need for replacing and sterilizing the entire device, thus saving costs.
[0084] In other words, in this embodiment, the treatment sleeve 11B can be a disposable item, and the extension section 12B and the portable unit 40B are an integrated structure that can be reused.
[0085] The treatment method (S100) of the penile erection bionic treatment system of the present invention is as follows:
[0086] (S101) The treatment sleeve 11 is fitted onto the outside of the patient's penis, and the portable unit 40 is fixed to the patient's waist;
[0087] (S102) The treatment sleeve 11 is connected to the portable unit 40 via the extension 12;
[0088] (S103) Operate the control panel 21 to start the vacuum pump 23 and the motor 24 according to the preset treatment temperature, preset treatment pressure and preset vibration frequency;
[0089] (S104) The treatment sleeve 11 and the monitoring unit 30 enter the working mode, and the monitoring unit 30 monitors the erection hardness and duration of the penis in real time;
[0090] (S105) The control unit 20 adjusts itself based on the data monitored by the monitoring unit 30 to adapt to the different needs of different patients; and
[0091] (S106) After the treatment, the patient operates the control panel 21 to turn off the penile erection bionic treatment system and releases the pressure of the negative pressure tube 121 and the negative pressure chamber 1104 through the pressure relief valve 125, so as to remove the treatment sleeve 10, complete the treatment operation, and discharge the liquid inside the negative pressure chamber 1104 and the negative pressure tube 121 through the liquid outlet 126.
[0092] In step (S102), the negative pressure connection end 122 and the motor connection end 124 of the extension section 12 are respectively connected to the negative pressure interface 44 and the motor interface 45 of the portable unit 40 to perform negative pressure therapy, heating therapy and massage therapy. Multiple treatment methods are used together to gently promote penile erection, prolong erection time, build patient confidence, and achieve the dual purpose of physical and psychological treatment.
[0093] In step (S103), the patient can operate the control panel 21 independently to activate the penile erection bionic treatment system according to the preset treatment temperature, treatment pressure, and vibration frequency, so that the massage bar 33, the electrode 34, and the vacuum pump 23 enter the corresponding working mode according to the preset instructions.
[0094] In steps (S104) and (S105), the monitoring unit 30 transmits data to the recording module 26 by monitoring the pressure, temperature and vibration of the penile surface. The processor 25 calculates the hardness and duration of penile erection based on the corresponding data, and sends instructions to the vacuum pump 23 and the motor 24 in a timely manner according to the preset hardness and duration requirements, so as to adjust the pressure, temperature and vibration frequency in a timely manner to meet the patient's needs.
[0095] It is worth mentioning that, under negative pressure, the liquid in the reservoir 48 enters the negative pressure chamber 1104 through the connecting pipe 49, the extension band 12, and gradually wraps around the penis during the liquid flow. Under the action of the massage strip 33, the penis is massaged, and under the action of the electrode 34, the liquid reaches 36-37°C, which is the same as the working temperature of the treatment sleeve 11. Multiple methods work synergistically to promote blood circulation in the penis and promote penile erection.
[0096] Those skilled in the art will understand that, in this invention, the portable penile erection bionic treatment system can be controlled via voice, buttons, remote control, or electronic devices. Negative pressure, heating, or vibration can be used individually, or simultaneously as needed. Liquid is injected under negative pressure, and the interaction of heating and vibration strengthens the corpora cavernosa, improves microcirculation, and allows more blood and nutrients to flow into the penis, accelerating corpora cavernosa engorgement, promoting corpora cavernosa cell division, thus facilitating penile erection and prolonging erection time. In addition to physiological treatment, it can be applied to sexual activity, building the patient's confidence psychologically. Through the dual effects of physiological and psychological approaches, a better therapeutic effect is achieved.
[0097] Those skilled in the art should understand that the embodiments of the present invention described above and shown in the accompanying drawings are merely examples and do not limit the present invention. The objectives of the present invention have been fully and effectively achieved. The functions and structural principles of the present invention have been demonstrated and explained in the embodiments, and any variations or modifications may be made to the implementation of the present invention without departing from the stated principles.
Claims
1. A portable penile erection bionic treatment system, characterized in that, include: A treatment unit includes a treatment sleeve and at least one extension connected to the rear end of the treatment sleeve. The treatment sleeve includes an inner shell, an outer shell, and a plurality of connectors. The connectors are connected between the inner shell and the outer shell, dividing the inner shell and the outer shell into a plurality of independent and closed connecting cavities and a plurality of negative pressure cavities. The treatment sleeve also has a fitting cavity, and the inner shell forms the outer wall of the fitting cavity for fitting onto the outside of the patient's penis. A portable unit, the portable unit including a portable body and a fitting surface, the fitting surface forming one side of the portable body to fit the patient's waist; A monitoring unit is installed inside the treatment sleeve to monitor the temperature, pressure, hardness, and duration of the penile surface; and A control unit is mounted on the portable body and connected to the treatment unit and the monitoring unit via the extension to send treatment commands.
2. The portable penile erection bionic treatment system according to claim 1, wherein the control unit includes a processor and a control panel, a vacuum pump, a motor and a recording module connected to the processor, the portable unit further includes a liquid storage tank and a connecting pipe communicating with the liquid storage tank, wherein the control panel is disposed on the surface of the portable body, and the vacuum pump, the motor, the processor, the recording module, the liquid storage tank and the connecting pipe are all disposed inside the portable body.
3. The portable penile erection bionic treatment system according to claim 2, wherein the portable unit has a negative pressure interface, a motor interface and a connecting pipe interface, which are respectively connected to the vacuum pump, the motor and the connecting pipe; the rear end of the extension section is provided with a negative pressure connection end, a motor connection end and a pipe connection end, which are respectively detachably connected to the negative pressure interface, the motor interface and the connecting pipe interface; the front end of the extension section is integrally formed with the treatment sleeve; wherein a negative pressure pipe is also provided inside the extension section, the negative pressure pipe is connected between the negative pressure connection end and the negative pressure chamber; the liquid storage tank is connected to the negative pressure chamber through the connecting pipe, the pipe connection end and the extension section; the extension section further includes a pressure relief valve, which is provided at the rear end of the extension section, wherein the pressure relief valve is connected to the negative pressure pipe.
4. The portable penile erection bionic treatment system according to claim 2, wherein the rear end of the extension section is integrally formed with the portable body, the front end of the extension section is detachably connected to the treatment sleeve, wherein the front end of the extension section is provided with a negative pressure connection end, a motor connection end and a tube connection end, which are respectively connected to the vacuum pump, the motor and the connecting tube, the treatment unit has a negative pressure interface, a motor interface and a connecting tube interface, which are respectively arranged adjacent to each other at the rear end of the treatment sleeve, and are respectively detachably connected to the negative pressure interface, the motor interface and the connecting tube interface, wherein the negative pressure interface and the connecting tube interface are both connected to the negative pressure chamber, the motor interface is electrically connected to the monitoring unit, the portable unit further includes a pressure relief valve, the pressure relief valve is disposed on the portable body and connected to the negative pressure tube.
5. The portable penile erection bionic treatment system according to claim 3 or 4, wherein the monitoring unit includes at least one temperature sensor, at least one pressure sensor, at least one massage strip and at least one electrode, wherein the temperature sensor and the pressure sensor are respectively installed in the connecting cavity, and the massage strip and the electrode are installed alternately on the outer wall of the inner shell, wherein the monitoring unit is connected to the control unit through the extension section, receives instructions from the control unit and performs corresponding operations.
6. The portable penile erection bionic treatment system according to claim 5, wherein the treatment sleeve further has an interface and an opening, the interface and the opening being respectively disposed at the rear end and the front end of the treatment sleeve, both communicating with the sleeve cavity, wherein the treatment sleeve is made of a flexible elastic material, the portable unit further includes a power supply, the power supply being disposed in the portable body and electrically connected to the control unit, the control unit further includes a voice control unit, the voice control unit being connected to the processor, wherein the voice control unit includes a prompter, a microphone and an alarm, the prompter, the microphone and the alarm being disposed in the portable body to establish a communication link between the operator and the processor.
7. The portable penile erection bionic treatment system according to claim 6, wherein the massage strip and the electrode are both strip-shaped, longitudinally arranged inside the treatment sleeve, and electrically connected to the motor and the processor, and the plurality of negative pressure chambers are longitudinally arranged in the treatment sleeve.
8. The portable penile erection bionic treatment system according to claim 6, wherein the massage strip and the electrode are both strip-shaped and are arranged in a ring inside the treatment sleeve, the negative pressure chamber includes two longitudinal negative pressure chambers and a plurality of annular negative pressure chambers, one of the longitudinal negative pressure chambers is connected to the vacuum pump through the extension section, the other longitudinal negative pressure chamber is connected to the liquid storage tank through the extension section, and the annular negative pressure chamber surrounds the treatment sleeve and communicates with the longitudinal negative pressure chambers.
9. A method for operating a portable penile erection bionic treatment system, characterized in that, Includes the following steps: (A) A portable unit is fixed to the patient's waist by attaching a treatment sleeve to the outside of the patient's penis, and the treatment sleeve is connected to the portable unit; (B) Operate a control panel and start a control unit according to the preset treatment temperature, treatment pressure and vibration frequency. The control unit sends a command to a monitoring unit, which is located inside the treatment sleeve. (C) The treatment sleeve and the monitoring unit enter the working mode according to the instructions. The monitoring unit monitors the temperature, pressure, erection hardness and duration of the patient's penis in real time and feeds it back to the control unit and the patient. as well as (D) The control unit adjusts itself based on the data fed back by the monitoring unit to adapt to the different needs of different patients.
10. The method of operating the portable penile erection bionic treatment system according to claim 9, wherein the method of operating further includes a step (E): after treatment, the portable penile erection bionic treatment system is turned off, and the pressure of a negative pressure tube and at least one negative pressure chamber included in the treatment unit is released through a pressure relief valve, and the treatment sleeve is removed, wherein in the above step, the monitoring unit includes at least one pressure sensor, at least one temperature sensor, at least one massage strip and at least one electrode, all of which are disposed in the treatment sleeve, the treatment sleeve also has at least one negative pressure chamber connected to the vacuum pump of the control unit to realize negative pressure and liquid injection, wherein the treatment sleeve is made of a flexible material, wraps around and fits the outside of the patient's penis and changes with the changes of the penis.