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Clinical Efficacy and Safety of Robot-assisted Total Knee Arthroplasty

U

University of Science and Technology of China (USTC)

Status

Enrolling

Conditions

Osteoarthritis, Knee

Treatments

Procedure: Conventional total knee arthroplasty
Procedure: Robot-assisted surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT06856356
XJS2023-1-18(WK)

Details and patient eligibility

About

The purpose of this clinical trial is to understand the application value of the Orthopedic Joint Surgery Navigation System in assisting surgeons to accurately place prosthetic components in adult knee replacement surgery. It will also confirm its effectiveness and safety in clinical application.

Full description

The purpose of this clinical trial is to understand the application value of the Orthopedic Joint Surgery Navigation System in assisting surgeons to accurately place prosthetic components in adult knee replacement surgery. It will also confirm its effectiveness and safety in clinical application. The main questions it aims to answer are:

Does the Orthopedic Joint Surgery Navigation System improve the accuracy of prosthetic component placement in knee replacement surgery? Is the Orthopedic Joint Surgery Navigation System superior to traditional total knee replacement What medical problems do participants encounter when taking medication ABC? Researchers will compare the Orthopedic Joint Surgery Navigation System with traditional total knee replacement surgery (using a "four-in-one" osteotomy guide) to see if the Orthopedic Joint Surgery Navigation System is superior to traditional total knee replacement in terms of prosthesis three-dimensional position, force alignment, patient satisfaction, functional scores, complications, etc.

Participants will:

End-stage knee osteoarthritis patients receive total knee replacement with the Orthopedic Joint Surgery Navigation System or traditional total knee replacement surgery Visit the clinic for examination and testing every 3 months Record their imaging data, satisfaction, functional scores, complications, etc.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subjects voluntarily participate in the trial and sign the informed consent form;
  2. Aged 18 to 80 years old (inclusive), regardless of gender;
  3. Patients who need total knee replacement surgery;
  4. Those who can communicate well with the researchers and comply with the trial requirements.

Exclusion criteria

  1. Patients who are allergic to the drugs used in this trial or the implant materials;
  2. Patients with immature bone development;
  3. Patients with active infection;
  4. Patients with neuropathy of the knee joint;
  5. Patients with poor bone quality that is not conducive to prosthesis fixation;
  6. Patients with general conditions or concomitant diseases that make it difficult for people to tolerate surgery;
  7. Patients with insufficient quadriceps muscle strength;
  8. Patients with insufficient skin coverage near the surgical site and intolerance to surgery;
  9. Patients with severe femoral or tibial deformities and other severe deformities outside the joint;
  10. Patients with metal implants in the joint surgical area that affect the execution of the surgical plan;
  11. Pregnant or lactating women;
  12. Patients with severe epilepsy or mental illness;
  13. Patients with alcohol dependence or drug addiction;
  14. Patients with severe coagulation disorders;
  15. Patients who have participated in or are participating in other clinical trials within one month of enrollment;
  16. Patients who are considered by the researchers to be unsuitable for participating in this clinical trial for other reasons. Those who meet any of the above exclusion criteria need to be excluded.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

Robot-assisted total knee arthroplasty
Experimental group
Description:
Using an orthopedic joint surgery navigation system to assist total knee replacement
Treatment:
Procedure: Robot-assisted surgery
Conventional total knee arthroplasty
Active Comparator group
Description:
Using a conventional 4-in-1 osteotomy guide for total knee replacement
Treatment:
Procedure: Conventional total knee arthroplasty

Trial contacts and locations

1

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Central trial contact

Xianyue Shen, M.D; Xianzuo Zhang, Ph.D

Data sourced from clinicaltrials.gov

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