101 results about "Cervical canal" patented technology

A method and system of providing therapy to a patient's uterus. The method includes the following steps: inserting an access tool through a cervix and a cervical canal into the uterus; after inserting the access tool into the uterus, creating a seal between an exterior surface of the access tool and an interior cervical os; providing an indication to a user that the seal has been created; delivering vapor through the access tool lumen into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool with a lumen, the access tool being adapted to be inserted through a human cervical canal to place an opening of the lumen within a uterus when the access tool is inserted through the cervical canal; a seal disposed at a distal region of the access tool and adapted to seal the access tool against an interior cervical os; a sealing indicator adapted to provide a user with an indication that the seal has sealed the access tool with the interior cervical os; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus.

An inflatable system, of between one and three balloons, for cervical dilation and labor induction is provided. The inflatable system may have a uterine balloon, for positioning at a proximal portion of the uterus, with respect to an operator, adjacent to the cervical internal os, the uterine balloon being shaped so as to maximize the pressure against the decidua and the internal cervical os and so as to minimize the pressure on the fetal head. Additionally or alternatively, the inflatable system may have a vaginal balloon, for positioning in the vagina, for applying pressure on the external cervical os. Additionally or alternatively, the inflatable system may have a cervical balloon, for positioning in the cervical canal, the cervical balloon being shaped so as to maximize the contact area with the cervix. The balloons are operative to stimulate the secretion of hormone, by exerting pressure on the proximal decidual surfaces of the uterus and on the cervix, so as to soften and ripen the cervix, cause the cervix to dilate, and induce labor. The balloons, which may have rough external surfaces, in order to keep them anchored in place, may be inflated by the operator, directly after their insertion, or manually and gradually, by the woman herself. Various sensors and other instruments may be used with the inflatable system, to monitor cervical dilation, fetal well-being, and the woman's conditions.

A device and method for dilating a cervical canal. The device includes an elongated member with an expandable anchoring component attached to its distal tip. An expandable dilating member is attached to the elongated member proximally of the anchoring component for dilating the cervical canal. The anchoring component can be expanded after insertion of the device into the cervical canal to correctly position the device relative to the canal. A device and method for sealing a cervical canal is also provided. The device includes a tube having an expandable seal assembly attached to its distal end. The seal assembly has a ridged or corrugated surface when it is in an expanded condition to provide a seal for the cervical canal.

A cervical canal dilating assembly and method of use are shown. The dilator assembly includes a plastic shaft, a first inflatable member, and a second inflatable member. The shaft can range from being rigid to being highly flexible. The second inflatable member is fabricated of a non-elastic material and is configured to have a maximum inflatable diameter. The second inflatable member is configured to have a predetermined maximum inflatable diameter ranging from 4 to 20 mm. The dilating assembly can also be at least partially covered by a sheath. A control system includes means for measuring pressure configured for at least monitoring the pressure of the second inflatable member. A wire can be used in selected configurations to stiffen and shape the shaft. In operation, the initial penetration of the dilating assembly into the uterus uses a wire for increased stiffness. The dilating assembly is then forwarded through the remainder of the cervical canal. The first inflatable member is expanded in the uterus after being uncovered by the sheath. The second inflatable member is positioned in the cervical canal and gradually inflated to a predetermined maximum diameter.

A method and system of providing therapy to a patient's uterus. In some embodiments the method includes the steps of: inserting an access tool through a cervix and a cervical canal into the uterus; placing an expansion mechanism in contact with tissue within the uterus to move uterine tissue surfaces away from an opening in an access tool lumen; delivering vapor through the vapor delivery tool into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool adapted to be inserted through a human cervical canal to place an opening of an access tool lumen within a uterus when the access tool is inserted through the cervical canal; an expansion mechanism adapted to be advanced into the uterus to move uterine tissue surfaces away from the opening in the access tool lumen; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus.

A cervical canal dilating assembly and method of use are shown. The dilator assembly includes a plastic shaft, a first inflatable member, and a second inflatable member. The shaft can range from being rigid to being highly flexible. The second inflatable member is fabricated of a non-elastic material and is configured to have a maximum inflatable diameter. The second inflatable member is configured to have a predetermined maximum inflatable diameter ranging from 4 to 20 mm. The dilating assembly can also be at least partially covered by a sheath. A control system includes means for measuring pressure configured for at least monitoring the pressure of the second inflatable member. A wire can be used in selected configurations to stiffen and shape the shaft. In operation, the initial penetration of the dilating assembly into the uterus uses a wire for increased stiffness. The dilating assembly is then forwarded through the remainder of the cervical canal. The first inflatable member is expanded in the uterus after being uncovered by the sheath. The second inflatable member is positioned in the cervical canal and gradually inflated to a predetermined maximum diameter.

A uterus manipulator includes a shank, in which a hollow probe is guided, whose distal end section is envisaged and designed for introduction into a uterus through the cervical canal. A handle is provided on the proximal side. A distally open bell and a vaginal seal, arranged proximally displaced thereto, as well as a suction channel which connects to at least one suction opening in the distal end section, are provided for receiving a cervix. The bell is designed as a suction bell, wherein at least one suction channel runs into the bell.

Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO2) through the probe into the uterine cavity and monitoring the rate of the flow to characterize the uterine cavity as perforated or non-perforated based on a change in the flow rate. If the flow rate drops to zero or close to zero, this indicates that the uterine cavity is intact and not perforated. If the flow rate does not drop to zero or close to zero, this indicates that a fluid flow is leaking through a perforation in the uterine cavity into the uterine cavity or escaping around an occlusion balloon that occludes the cervical canal.

Methods, systems and devices for endometrial ablation. In accordance with a method, a working end of an RF ablation device is positioned in a patient uterus to contact endometrial tissue, the working end comprising a dielectric wall capable of non-expanded and expanded shapes. A sealing member is deployed in the cervical canal during ablation.

The device consists of a shaft with a detachable brush head. The brush head is a new design incorporating the utility of an expandable self adjusting area that yields a complete sample of the endocervix and exocervix regardless of varying individual anatomy. The brush head has protrusions disposed at strategic positions with flat surface collection areas. A ledge with protrusions samples the exocervical area and a middle portion samples the endocervical area. The middle portion automatically elongates from approximately 2 cm to 5.5 cm as to adjust to individual anatomies as the brush head is inserted into the cervical canal. The brush head is matched to a special collection container that permits the brush head to be detached and deposited into the container without the handling of the brush / head area. The special conical insert within the container automatically orients brush head for passage through horizontal slot at bottom of insert without operator's need to manually align. In this fashion the sampled cellular material can be completely, safely, and securely transported for laboratory evaluation.

A method and system of providing therapy to a patient's uterus. The method includes the steps of inserting an access tool through a cervix and a cervical canal into the uterus; actively cooling the cervical canal; delivering vapor through the access tool lumen into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool with a lumen, the access tool being adapted to be inserted through a human cervical canal to place an opening of the lumen within a uterus when the access tool is inserted through the cervical canal; an active cooling mechanism adapted to cool the cervical canal, the active cooling mechanism having a coolant source; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus.

A device and method for dilating a cervical canal. The device includes an elongated member with an expandable anchoring component attached to its distal tip. An expandable dilating member is attached to the elongated member proximally of the anchoring component for dilating the cervical canal. The anchoring component can be expanded after insertion of the device into the cervical canal to correctly position the device relative to the canal. A device and method for sealing a cervical canal is also provided. The device includes a tube having an expandable seal assembly attached to its distal end. The seal assembly has a ridged or corrugated surface when it is in an expanded condition to provide a seal for the cervical canal.

A method and system of providing therapy to a patient's uterus. The method include the following steps: inserting an access tool through a cervix and a cervical canal into the uterus; after inserting the access tool into the uterus, inserting a vapor delivery tool through an access tool lumen; delivering vapor through the vapor delivery tool into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool, the access tool being adapted to be inserted through a human cervical canal to place an opening of the access tool lumen within a uterus when the access tool is inserted through the cervical canal; and a vapor delivery mechanism, the vapor delivery mechanism having a vapor delivery tool and a vapor source, the vapor delivery tool being adapted to be inserted through the access tool to deliver condensable vapor from the vapor source to the uterus, the condensable vapor being adapted to condense within the uterus.

Methods, systems and devices for endometrial ablation. In accordance with a method, a working end of an RF ablation device is positioned in a patient uterus to contact endometrial tissue, the working end comprising a dielectric wall capable of non-expanded and expanded shapes. An indicator mechanism is operatively coupled to the wall and configured to indicate non-expanded and expanded shapes of the wall. An expandable member, such as a balloon, is provided that expands to close the cervical canal during ablation.

A device useful in forming a seal between a hysteroscope instrument and a cervical canal during diagnostic or surgical procedures known as hysteroscopy. The device grasps the exterior of the cervical canal pressing the cervical canal inwardly toward the outer surface of the hysteroscope instrument forming a seal between the outer surface of the hysteroscope instrument and the cervical canal, thereby preventing fluid or gas from exiting the cervical canal.

A system for treating uterine tissue having a seal assembly configured for positioning in a patient's cervical canal and uterine cavity; an expandable distal balloon portion; an expandable elongate medial balloon portion configured for movement between a first transversely expanded shape for engaging a cervical canal and a second transversely non-expanded shape for trans-cervical insertion; and a fluid source in communication with distal balloon portion and medial balloon portion for expansion of said balloon portions.

A cervical canal dilator having an elongate tubular shaft that defines at least two internal lumens that are juxtaposed to a longitudinal axis. A first inflatable member is positioned on the outer surface of the shaft and is in communication with the first lumen. While a second inflatable member is also positioned on the outer surface of the shaft. The second inflatable, however, is longer than and completely covers the first inflatable member. Additionally, the second member is fabricated of a non-elastic material that limits the inflation of the second member to a predetermined maximum diameter of inflation. The device, also, has a control system which controls the fluids and / or gases that enter the lumens.

A method and system of providing therapy to a patient's uterus. The method include the following steps: inserting an access tool through a cervix and a cervical canal into the uterus; after inserting the access tool into the uterus, inserting a vapor delivery tool through an access tool lumen; delivering vapor through the vapor delivery tool into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool, the access tool being adapted to be inserted through a human cervical canal to place an opening of the access tool lumen within a uterus when the access tool is inserted through the cervical canal; and a vapor delivery mechanism, the vapor delivery mechanism having a vapor delivery tool and a vapor source, the vapor delivery tool being adapted to be inserted through the access tool to deliver condensable vapor from the vapor source to the uterus, the condensable vapor being adapted to condense within the uterus.

Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO2) through the probe into the uterine cavity and monitoring the rate of the flow to characterize the uterine cavity as perforated or non-perforated based on a change in the flow rate. If the flow rate drops to zero or close to zero, this indicates that the uterine cavity is intact and not perforated. If the flow rate does not drop to zero or close to zero, this indicates that a fluid flow is leaking through a perforation in the uterine cavity into the uterine cavity or escaping around an occlusion balloon that occludes the cervical canal.

A method and system of providing therapy to a patient's uterus. In some embodiments the method includes the steps of: inserting an access tool through a cervix and a cervical canal into the uterus; placing an expansion mechanism in contact with tissue within the uterus to move uterine tissue surfaces away from an opening in an access tool lumen; delivering vapor through the vapor delivery tool into the uterus; and condensing the vapor on tissue within the uterus. The system has an access tool adapted to be inserted through a human cervical canal to place an opening of an access tool lumen within a uterus when the access tool is inserted through the cervical canal; an expansion mechanism adapted to be advanced into the uterus to move uterine tissue surfaces away from the opening in the access tool lumen; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus.

The invention relates to a cervix brush, comprising a sheath tube, a core pole, a scraper, villus and a guiding head; wherein, the scraper, the guiding head and the sheath tube are formed by integrated injection molding, the guiding head is arranged at the foremost end of the sheath tube, the scraper comprises six plastic strips which can be detached to triangles, the front end of the scraper is connected with the guiding head, the back end of the scraper is connected with the sheath tube and a easy folded groove is arranged between the connection and the scraper, the core pole is axially sleeved in the sheath tube and is slideable, the head of the core pole is fixed in the guiding head, the villus is cultivated at the front ends of the guiding head, the scraper and the sheath tube, the stress on the surface of the cervix from the six scrapers which can be furled and spread is uniform, in particular that the cells at area with high incidence of the cervical cancer from the one third part outside of the cervical canal to the external cervical orifice can be gotten by the cervix brush. The cervix brush has the advantages of small radial direction size, convenient operation and low manufacturing cost.

Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO2) through the probe into the uterine cavity and monitoring the rate of the flow to characterize the uterine cavity as perforated or non-perforated based on a change in the flow rate. If the flow rate drops to zero or close to zero, this indicates that the uterine cavity is intact and not perforated. If the flow rate does not drop to zero or close to zero, this indicates that a fluid flow is leaking through a perforation in the uterine cavity into the uterine cavity or escaping around an occlusion balloon that occludes the cervical canal.

A device useful in diagnostic or surgical procedures for sealing the cervical canal in which an inflatable device is used with a hysteroscope instrument. The inflatable device provides a seal between an outer surface of the hysteroscope instrument and the cervical canal, thereby preventing fluids from exiting the cervical canal.

A cervical canal dilating assembly and method of use are shown. The dilator assembly includes a plastic shaft, a first inflatable member, and a second inflatable member. The shaft can range from being rigid to being highly flexible. The second inflatable member is fabricated of a non-elastic material and is configured to have a maximum inflatable diameter. The second inflatable member is configured to have a predetermined maximum inflatable diameter ranging from 4 to 20 mm. The dilating assembly can also be at least partially covered by a sheath. A control system includes means for measuring pressure configured for at least monitoring the pressure of the second inflatable member. A wire can be used in selected configurations to stiffen and shape the shaft. In operation, the initial penetration of the dilating assembly into the uterus uses a wire for increased stiffness. The dilating assembly is then forwarded through the remainder of the cervical canal. The first inflatable member is expanded in the uterus after being uncovered by the sheath. The second inflatable member is positioned in the cervical canal and gradually inflated to a predetermined maximum diameter.

A uterus manipulator includes a shank, in which a hollow probe is guided, whose distal end section is envisaged and designed for introduction into a uterus through the cervical canal. A handle is provided on the proximal side. A distally open bell and a vaginal seal, arranged proximally displaced thereto, as well as a suction channel which connects to at least one suction opening in the distal end section, are provided for receiving a cervix. The bell is designed as a suction bell, wherein at least one suction channel runs into the bell.

A device serves for performing examination and surgical intervention on the uterus. The device comprises an approximate rod-shaped body and an extension piece protruding from a distal end of said body. Said extension piece can be introduced in a cervical canal of an uterus. At least one adjustable jaw part for fixing of a cervical tissue between said extension piece and said jaw part is provided. An operating device serves for operating said adjustable jaw part. Said operating device is arranged on said rod-shaped body in such a way that a hand of an operator gripping said body can operate said operating device.

Methods, systems and devices for endometrial ablation. In accordance with a method, a working end of an RF ablation device is positioned in a patient uterus to contact endometrial tissue, the working end comprising a dielectric wall capable of non-expanded and expanded shapes. An indicator mechanism is operatively coupled to the wall and configured to indicate non-expanded and expanded shapes of the wall. An expandable member, such as a balloon, is provided that expands to close the cervical canal during ablation.