Spinal cord injury therapeutic agent treatment reaction monitoring device

By designing a spinal cord injury treatment response monitoring device with motor-driven gears and rack system, the problem that existing devices cannot adjust the position of push plates and foot plates is solved, and monitoring effects suitable for different leg thicknesses and lengths are achieved.

CN119700028APending Publication Date: 2025-03-28JIANGSU RE STEM BIOTECH
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
CN202411904185.9
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-12-23
Publication Date
2025-03-28

AI Technical Summary

Technical Problem

The existing spinal cord injury therapeutic agent treatment response monitoring device cannot facilitate the adjustment of the position of the push plate and foot plate, resulting in the inability to be applied to legs of different thicknesses and lengths.

Method used

A device including a support assembly, a leg edema monitoring assembly, a foot edema monitoring assembly, a guide assembly and an adjustment assembly is designed to realize the position adjustment of the leg and foot fitting frame through the motor driving the gear and rack system.

Benefits of technology

The position of the leg and foot fitting rack is adjusted according to the thickness and length of the patient's legs, which is suitable for the needs of different patients and improves the accuracy and flexibility of monitoring.

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure CN119700028A_ABST
    Figure CN119700028A_ABST
Patent Text Reader

Abstract

The invention discloses a spinal cord injury therapeutic agent treatment response monitoring device, and belongs to the technical field of spinal cord injury treatment, and the spinal cord injury therapeutic agent treatment response monitoring device comprises a supporting assembly used for supporting the legs of a patient; the leg edema monitoring assembly is used for monitoring the reaction condition of leg edema of the patient; the first guide assembly is used for guiding and limiting the leg edema monitoring part; the first adjusting assembly is used for adjusting the position of the leg edema monitoring part; the foot edema monitoring assembly is used for monitoring the reaction condition of foot edema of the patient; the rotating assembly is used for driving the first adjusting assembly and the second adjusting assembly; the second adjusting assembly is used for adjusting the foot edema monitoring assembly. By arranging the motor, the motor is started to drive the first rotating rod to rotate, the first rotating rod rotates to drive the first gear to rotate, the first gear rotates to drive the first rack to move, then the leg attaching frame can be conveniently driven to move to be attached to the legs of the patient, and the position of the leg attaching frame can be conveniently adjusted according to the thickness of the legs of the patient.
Need to check novelty before this filing date? Find Prior Art

Description

Technical Field

[0001] The invention relates to a treatment response monitoring device, in particular to a treatment response monitoring device for spinal cord injury therapeutic agent, and belongs to the technical field of spinal cord injury treatment. Background Art

[0002] When the spinal cord is injured, the patient's legs are prone to edema. In this case, therapeutic agents are needed for treatment. After using the therapeutic agents, a reaction monitoring device is needed to observe the patient's treatment status.

[0003] However, in actual use, the existing spinal cord injury therapeutic agent treatment response monitoring device cannot easily adjust the position of the push plate, thereby making it inconvenient to use for patients with different leg thicknesses, and cannot easily adjust the position of the foot plate, thereby making it inconvenient to use for patients with different leg lengths. Summary of the invention

[0004] The main purpose of the present invention is to solve the problem that the position of the push plate and the position of the foot plate cannot be easily adjusted, and to provide a spinal cord injury therapeutic agent treatment response monitoring device.

[0005] The purpose of the present invention can be achieved by adopting the following technical solutions:

[0006] A spinal cord injury therapeutic agent treatment response monitoring device, comprising

[0007] A support assembly for supporting the patient's legs;

[0008] A leg edema monitoring component is used to monitor the patient's leg edema response;

[0009] A first guide component, used for guiding and limiting the leg edema monitoring component;

[0010] A first adjustment component, used for adjusting the position of the leg edema monitoring component;

[0011] A foot edema monitoring component, used to monitor the patient's foot edema response;

[0012] A rotating assembly, used to drive the first adjusting assembly and the second adjusting assembly;

[0013] A second adjustment component, used for adjusting a foot edema monitoring component;

[0014] The second guide component is used to guide and limit the foot edema monitoring component.

[0015] Preferably, the support assembly comprises a support frame, a support plate, support legs and a placement plate, the support frame is provided with a support plate, the top of the support plate is equipped with support legs, and the placement plate is equipped with a placement plate on the top of the support legs.

[0016] Preferably, the first guide assembly includes a first guide rod, a guide ring and a first connecting rod, the first guide rods are installed on both sides of the support plate, one end of the first guide rod is connected to the support frame, a guide ring is slidably installed on the first guide rod, the guide ring is installed on the first connecting rod, and one end of the first connecting rod is connected to the leg edema monitoring assembly.

[0017] Preferably, the leg edema monitoring component includes a support plate, a guide rod, a first spring, a first pressure sensor and a leg fitting frame, a support plate is installed at one end of the first connecting rod, the first pressure sensor is installed on the support plate, a guide rod is slidably installed on the support plate, the leg fitting frame is installed at one end of the guide rod, and the leg fitting frame is connected to the support plate via a first spring.

[0018] Preferably, the rotating assembly includes a motor, a motor support frame and a support frame connecting column, the support frame is mounted on the support frame, one end of the support frame connecting column is mounted with a motor support frame, and the motor is mounted on the motor support frame.

[0019] Preferably, the first adjustment component includes a connecting column, a first rack, a first gear and a first rotating rod, the connecting column is installed on the support plate, the first rack is installed at one end of the connecting column, the first rotating rod is installed at the output end of the motor, the first gear is installed on the first rotating rod, and the first rack meshing with the first gear is installed on the connecting column.

[0020] Preferably, a support ring connecting column is installed on the support frame, a support ring is installed on one end of the support ring connecting column, the first rotating rod is rotatably connected to the support ring, and one end of the first rotating rod is connected to the support frame via a bearing.

[0021] Preferably, the second guide assembly includes a limit column, a limit ring and a bottom rod, the support plate is connected to the support frame via the limit column, the limit ring is slidably installed on the limit column, the bottom rod is installed on the top of the limit ring, and a foot edema monitoring assembly is installed on one end of the bottom rod.

[0022] Preferably, the foot edema monitoring component includes a support bar, a foot connecting plate, a connecting plate, a guide column, a side rod, a second spring and a second pressure sensor, the support bar is installed on the top of the bottom rod, the guide column is slidably installed on the support bar, a connecting plate is installed at one end of the guide column, a side rod is installed on the connecting plate, a foot connecting plate is installed at one end of the side rod, the foot connecting plate is connected to the support bar via a second spring, and the second pressure sensor is installed on the support bar.

[0023] Preferably, the second adjustment assembly includes a second gear, a second rack, a second connecting rod, a second rotating rod and a third gear. The second connecting rod is installed on the support bar, a second rack is installed on one end of the second connecting rod, a second rotating rod is rotatably installed on the support frame, the second rotating rod is installed on the third gear, the third gear is meshed with the second rack, the second gear is installed on the first rotating rod, and the second gear is meshed with the third gear.

[0024] Beneficial technical effects of the present invention:

[0025] 1. According to the spinal cord injury therapeutic agent treatment response monitoring device of the present invention, a motor is set up, and when the motor is started, the first rotating rod is driven to rotate, and when the first rotating rod rotates, the first gear is driven to rotate, and when the first gear rotates, the first rack is driven to move, thereby facilitating the movement of the leg fitting frame to fit the patient's legs, and the position of the leg fitting frame can be adjusted according to the thickness of the patient's legs.

[0026] 2. The motor starts to drive the first rotating rod to rotate, which can drive the second gear to rotate. When the second gear rotates, it can drive the third gear to rotate. When the third gear rotates, it drives the second rack to move, which can facilitate the movement of the foot connecting plate to fit the patient's foot. BRIEF DESCRIPTION OF THE DRAWINGS

[0027] Figure 1 It is a schematic diagram of the overall structure of the present invention;

[0028] Figure 2 It is a schematic diagram of the motor structure of the present invention;

[0029] Figure 3 is a schematic diagram of the first gear structure of the present invention;

[0030] Figure 4 is a schematic diagram of the third gear structure of the present invention;

[0031] Figure 5 It is a schematic diagram of the first rack structure of the present invention;

[0032] Figure 6 It is a schematic diagram of the structure of the leg fitting frame of the present invention;

[0033] Figure 7 It is a schematic diagram of the guide ring structure of the present invention;

[0034] Figure 8 It is a schematic diagram of the structure of the limiting ring of the present invention;

[0035] Fig. 9 is a schematic diagram of the second rotating rod structure of the present invention;

[0036] Fig.10It is a schematic diagram of the support ring structure of the present invention.

[0037] In the figure: 1. support frame; 11. support plate; 12. support leg; 13. placement plate; 2. first guide rod; 21. guide ring; 22. first connecting rod; 3. support plate; 31. guide rod; 32. first spring; 34. first pressure sensor; 35. leg fitting frame; 4. connecting column; 41. first rack; 42. first gear; 43. first rotating rod; 5. support bar; 51. foot connecting plate; 52. connecting plate; 53. guide column; 54. side rod; 55. second spring; 56. second pressure sensor; 6. motor; 61. motor support frame; 62. support frame connecting column; 7. support ring; 71. support ring connecting column; 8. second gear; 81. second rack; 82. second connecting rod; 83. second rotating rod; 84. third gear; 9. limit column; 91. limit ring; 92. bottom rod. DETAILED DESCRIPTION

[0038] In order to make the technical solution of the present invention more clear and specific to those skilled in the art, the present invention is further described in detail below in conjunction with embodiments and drawings, but the implementation manner of the present invention is not limited thereto.

[0039] like Figure 1-Figure 10As shown, the spinal cord injury therapeutic agent treatment response monitoring device provided in this embodiment includes a support component for supporting the patient's legs; a leg edema monitoring component for monitoring the reaction status of the patient's leg edema; a first guide component for guiding and limiting the leg edema monitoring component; a first adjustment component for adjusting the position of the leg edema monitoring component; a foot edema monitoring component for monitoring the reaction status of the patient's foot edema; a rotating component for driving the first adjustment component and the second adjustment component; a second adjustment component for adjusting the foot edema monitoring component; a second guide component for guiding and limiting the foot edema monitoring component, and the support component includes a support frame 1, a support plate 11, a support leg 12 and a placement plate 13, and the support frame 1 is provided with a support plate 11 A support leg 12 is installed on the top of the support plate 11, and a placement plate 13 is installed on the top of the support leg 12. The first guide assembly includes a first guide rod 2, a guide ring 21 and a first connecting rod 22. The first guide rods 2 are installed on both sides of the support plate 11, one end of the first guide rod 2 is connected to the support frame 1, and a guide ring 21 is slidably installed on the first guide rod 2, and the first connecting rod 22 is installed on the guide ring 21. One end of the first connecting rod 22 is connected to the leg edema monitoring assembly, and the leg edema monitoring assembly includes a support plate 3, a guide rod 31, a first spring 32, a first pressure sensor 34 and a leg fitting frame 35. A support plate 3 is installed on one end of the first connecting rod 22, and the first pressure sensor 34 is installed on the support plate 3. A guide rod 31, one end of which is provided with a leg fitting frame 35, the leg fitting frame 35 is connected to the support plate 3 through a first spring 32, the rotating assembly comprises a motor 6, a motor support frame 61 and a support frame connecting column 62, the support frame 1 is provided with a support frame connecting column 62, one end of the support frame connecting column 62 is provided with a motor support frame 61, the motor 6 is provided on the motor support frame 61, the first adjusting assembly comprises a connecting column 4, a first rack 41, a first gear 42 and a first rotating rod 43, the support plate 3 is provided with a connecting column 4, one end of the connecting column 4 is provided with a first rack 41, the output end of the motor 6 is provided with a first rotating rod 43, the first gear 42 is provided on the first rotating rod 43, and a first gear meshed with the first gear 42 is provided on the connecting column 4 A rack 41 is provided on the support frame 1, and a support ring connecting column 71 is provided on one end of the support ring connecting column 71. A first rotating rod 43 is rotatably connected to the support ring 7, and one end of the first rotating rod 43 is connected to the support frame 1 through a bearing. By setting a motor 6, the motor 6 starts to drive the first rotating rod 43 to rotate, and when the first rotating rod 43 rotates, it drives the first gear 42 to rotate, and when the first gear 42 rotates, it drives the first rack 41 to move, so that it can facilitate the movement of the leg fitting frame 35 to fit the patient's legs, and can facilitate the position of the leg fitting frame 35 to be adjusted according to the thickness of the patient's legs. By setting the leg fitting frame 35, when the leg fitting frame 35 fits the legs, the leg fitting frame 35 squeezes the first spring 32, and the first spring 32 shortens.One side of the leg fitting frame 35 fits with the first pressure sensor 34. When the patient's leg is swollen, the leg fitting frame 35 moves, the first spring 32 extends, and the leg fitting frame 35 is separated from the first pressure sensor 34, so that the swelling of the patient's leg can be monitored. By setting the first guide rod 2 and the guide ring 21 to be slidably connected, the leg fitting frame 35 can be guided and limited. By setting the guide rod 31 and the support plate 3 to be slidably connected, the leg fitting frame 35 can be guided and limited. By setting the connecting column 4, the first rack 41 can be supported. By setting the support ring connecting column 71 and the support ring 7, the first rotating rod 43 can be supported. By setting the motor support frame 61 and the support frame connecting column 62, the motor 6 can be supported.

[0040] In this embodiment, if Figure 1 , Figure 2 , Figure 4 , Figure 5 , Figure 8 , Fig. 9 and Fig.10As shown, the second guide assembly includes a limit column 9, a limit ring 91 and a bottom rod 92. The support plate 11 is connected to the support frame 1 through the limit column 9. The limit ring 91 is slidably installed on the limit column 9. The top of the limit ring 91 is installed with a bottom rod 92. One end of the bottom rod 92 is installed with a foot edema monitoring assembly. The foot edema monitoring assembly includes a support bar 5, a foot connecting plate 51, a connecting plate 52, a guide column 53, a side rod 54, a second spring 55 and a second press sensor 56. The top of the bottom rod 92 is installed with a support bar 5, and a guide bar is slidably installed on the support bar 5. The guide column 53 is provided with a connecting plate 52 at one end of the guide column 53, a side rod 54 is provided on the connecting plate 52, a foot connecting plate 51 is provided at one end of the side rod 54, the foot connecting plate 51 is connected to the support bar 5 through a second spring 55, a second pressing sensor 56 is provided on the support bar 5, the second adjusting component comprises a second gear 8, a second rack 81, a second connecting rod 82, a second rotating rod 83 and a third gear 84, a second connecting rod 82 is provided on the support bar 5, a second rack 81 is provided at one end of the second connecting rod 82, and a second rotating rod 83 is provided on the support frame 1. The second rotating rod 83 is installed with a third gear 84, and the third gear 84 is meshed with the second rack 81. The first rotating rod 43 is installed with a second gear 8, and the second gear 8 is meshed with the third gear 84. When the motor 6 is started, the first rotating rod 43 is driven to rotate, which can drive the second gear 8 to rotate. When the second gear 8 rotates, the third gear 84 is driven to rotate. When the third gear 84 rotates, the second rack 81 is driven to move, which can facilitate the foot connecting plate 51 to move and fit the patient's foot. By setting The foot connecting plate 51 fits the patient's foot, the second spring 55 is shortened, and the second pressure sensor 56 contacts the foot connecting plate 51. When the patient's leg swelling subsides, the second spring 55 extends to separate the foot connecting plate 51 from the second pressure sensor 56, so that the patient's edema can be monitored when the swelling subsides. By setting a guide column 53 that is slidably connected to the support bar 5, the foot connecting plate 51 can be guided and limited. By setting a limit ring 91 that is slidably connected to the limit column 9, the support bar 5 can be guided and limited.

[0041] In this embodiment, if Figure 1-Figure 10 As shown, the working process of a spinal cord injury therapeutic agent treatment response monitoring device provided in this embodiment is as follows:

[0042] Step 1: The motor 6 is started to drive the first rotating rod 43 to rotate. When the first rotating rod 43 rotates, it drives the first gear 42 to rotate. When the first gear 42 rotates, it drives the first rack 41 to move, thereby driving the leg fitting frame 35 to move and fit with the patient's legs. When the leg fitting frame 35 fits with the legs, the leg fitting frame 35 squeezes the first spring 32, the first spring 32 shortens, and one side of the leg fitting frame 35 fits with the first pressure sensor 34. When the patient's legs are swollen, the leg fitting frame 35 moves, the first spring 32 extends, and the leg fitting frame 35 is separated from the first pressure sensor 34, and the swelling of the patient's legs is detected.

[0043] Step 2: The motor 6 is started to drive the first rotating rod 43 to rotate, and then drive the second gear 8 to rotate. When the second gear 8 rotates, it drives the third gear 84 to rotate. When the third gear 84 rotates, it drives the second rack 81 to move, and then drives the foot connecting plate 51 to move and fit the patient's foot. The foot connecting plate 51 fits the patient's foot, the second spring 55 shortens, and the second pressure sensor 56 contacts the foot connecting plate 51. When the patient's leg swelling subsides, the second spring 55 extends to separate the foot connecting plate 51 from the second pressure sensor 56, so as to monitor the patient's edema when it subsides.

[0044] In summary, in this embodiment, according to the spinal cord injury therapeutic agent treatment response monitoring device of this embodiment, by setting the motor 6, the motor 6 is started to drive the first rotating rod 43 to rotate, and when the first rotating rod 43 rotates, it drives the first gear 42 to rotate, and when the first gear 42 rotates, it drives the first rack 41 to move, so that it is convenient to drive the leg fitting frame 35 to move and fit the patient's legs, and it is convenient to adjust the position of the leg fitting frame 35 according to the thickness of the patient's legs. By setting the leg fitting frame 35, when the leg fitting frame 35 is fitted with the legs, the leg fitting frame 35 5 squeezes the first spring 32, the first spring 32 shortens, and one side of the leg fitting frame 35 fits with the first pressing sensor 34. When the patient's leg swelling subsides, the leg fitting frame 35 moves, the first spring 32 extends, and the leg fitting frame 35 separates from the first pressing sensor 34, so that the swelling of the patient's leg can be monitored. By arranging the first guide rod 2 to be slidably connected with the guide ring 21, it is convenient to guide and limit the leg fitting frame 35. By arranging the guide rod 31 to be slidably connected with the support plate 3, it is convenient to guide and limit the leg fitting frame 35. By setting the connecting column 4, it is convenient to support the first rack 41, by setting the supporting ring connecting column 71 and the supporting ring 7, it is convenient to support the first rotating rod 43, by setting the motor support frame 61 and the supporting frame connecting column 62, it is convenient to support the motor 6, the motor 6 starts to drive the first rotating rod 43 to rotate, which can drive the second gear 8 to rotate, and when the second gear 8 rotates, it can drive the third gear 84 to rotate, and when the third gear 84 rotates, it drives the second rack 81 to move, so as to facilitate the foot connecting plate 51 to move and fit the patient's foot. By setting the foot connecting plate 51, the foot connecting plate 51 fits the patient's foot, the second spring 55 is shortened, and the second pressure sensor 56 contacts the foot connecting plate 51. When the patient's leg swelling subsides, the second spring 55 extends to separate the foot connecting plate 51 from the second pressure sensor 56, so that the patient's edema can be monitored when the swelling subsides. By setting the guide column 53 to be slidably connected with the support bar 5, it is convenient to guide and limit the foot connecting plate 51. By setting the limiting ring 91 to be slidably connected with the limiting column 9, it is convenient to guide and limit the support bar 5.

[0045] For example, certain words are used in the specification and claims to refer to specific components. Those skilled in the art should understand that hardware manufacturers may use different terms to refer to the same component. This specification and claims do not use differences in names as a way to distinguish components, but use differences in the functions of components as the criteria for distinction. For example, "including" mentioned throughout the specification and claims is an open term, so it should be interpreted as "including but not limited to". "Approximately" means that within an acceptable error range, those skilled in the art can solve technical problems within a certain error range and basically achieve technical effects.

[0046] It should be noted that the terms "include", "comprises" or any other variations thereof are intended to cover non-exclusive inclusion, so that a product or system including a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such product or system. In the absence of more restrictions, the elements defined by the sentence "comprises a ..." do not exclude the existence of other identical elements in the product or system including the elements.

[0047] The above description shows and describes several preferred embodiments of the present invention, but as mentioned above, it should be understood that the present invention is not limited to the form disclosed herein, and should not be regarded as excluding other embodiments, but can be used in various other combinations, modifications and environments, and can be modified within the scope of the invention concept described herein through the above teachings or the technology or knowledge of the relevant field. Changes and variations made by those skilled in the art do not depart from the spirit and scope of the present invention, and should be within the scope of protection of the claims attached to the present invention.

Claims

1. A spinal cord injury therapeutic agent treatment response monitoring device, characterized in that: include A support assembly for supporting the patient's legs; A leg edema monitoring component is used to monitor the patient's leg edema response; A first guide component, used for guiding and limiting the leg edema monitoring component; A first adjustment component, used for adjusting the position of the leg edema monitoring component; A foot edema monitoring component, used to monitor the patient's foot edema response; A rotating assembly, used to drive the first adjusting assembly and the second adjusting assembly; A second adjustment component, used for adjusting a foot edema monitoring component; The second guide component is used to guide and limit the foot edema monitoring component.

2. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 1, characterized in that: The support assembly comprises a support frame (1), a support plate (11), support legs (12) and a placement plate (13); the support frame (1) is provided with the support plate (11), the top of the support plate (11) is mounted with the support legs (12), and the top of the support legs (12) is mounted with the placement plate (13).

3. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 2, characterized in that: The first guide assembly comprises a first guide rod (2), a guide ring (21) and a first connecting rod (22); the first guide rods (2) are installed on both sides of the support plate (11); one end of the first guide rod (2) is connected to the support frame (1); a guide ring (21) is slidably installed on the first guide rod (2); a first connecting rod (22) is installed on the guide ring (21); one end of the first connecting rod (22) is connected to the leg edema monitoring assembly.

4. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 3, characterized in that: The leg edema monitoring component comprises a support plate (3), a guide rod (31), a first spring (32), a first pressure sensor (34) and a leg fitting frame (35); one end of the first connecting rod (22) is provided with a support plate (3); the first pressure sensor (34) is provided on the support plate (3); a guide rod (31) is slidably provided on the support plate (3); one end of the guide rod (31) is provided with a leg fitting frame (35); the leg fitting frame (35) is connected to the support plate (3) via a first spring (32).

5. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 4, characterized in that: The rotating assembly comprises a motor (6), a motor support frame (61) and a support frame connecting column (62); the support frame connecting column (62) is mounted on the support frame (1); the motor support frame (61) is mounted on one end of the support frame connecting column (62); and the motor (6) is mounted on the motor support frame (61).

6. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 5, characterized in that: The first adjustment component comprises a connecting column (4), a first rack (41), a first gear (42) and a first rotating rod (43); the connecting column (4) is mounted on the support plate (3); one end of the connecting column (4) is mounted with the first rack (41); the output end of the motor (6) is mounted with the first rotating rod (43); the first gear (42) is mounted on the first rotating rod (43); and the connecting column (4) is mounted with the first rack (41) meshing with the first gear (42).

7. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 6, characterized in that: A support ring connecting column (71) is installed on the support frame (1), a support ring (7) is installed on one end of the support ring connecting column (71), the first rotating rod (43) is rotatably connected to the support ring (7), and one end of the first rotating rod (43) is connected to the support frame (1) via a bearing.

8. The device for monitoring the therapeutic response of a spinal cord injury therapeutic agent according to claim 6, characterized in that: The second guide assembly comprises a limiting column (9), a limiting ring (91) and a bottom rod (92); the support plate (11) is connected to the support frame (1) via the limiting column (9); the limiting ring (91) is slidably mounted on the limiting column (9); the bottom rod (92) is mounted on the top of the limiting ring (91); and a foot edema monitoring assembly is mounted on one end of the bottom rod (92).

9. A spinal cord injury therapeutic agent treatment response monitoring device according to claim 8, characterized in that: The foot edema monitoring component comprises a support bar (5), a foot connecting plate (51), a connecting disk (52), a guide column (53), a side rod (54), a second spring (55) and a second pressure sensor (56); the support bar (5) is installed on the top of the bottom rod (92); the guide column (53) is slidably installed on the support bar (5); one end of the guide column (53) is installed with a connecting disk (52); the connecting disk (52) is installed with a side rod (54); one end of the side rod (54) is installed with a foot connecting plate (51); the foot connecting plate (51) is connected to the support bar (5) via a second spring (55); and the support bar (5) is installed with a second pressure sensor (56).

10. The device for monitoring the therapeutic response of a spinal cord injury therapeutic agent according to claim 9, characterized in that: The second adjustment component comprises a second gear (8), a second rack (81), a second connecting rod (82), a second rotating rod (83) and a third gear (84); the second connecting rod (82) is mounted on the support bar (5); a second rack (81) is mounted on one end of the second connecting rod (82); a second rotating rod (83) is rotatably mounted on the support frame (1); a third gear (84) is mounted on the second rotating rod (83); the third gear (84) is meshingly connected with the second rack (81); a second gear (8) is mounted on the first rotating rod (43); the second gear (8) is meshingly connected with the third gear (84).