Evaluation of the patient reported outcomes after sensor-guided total knee arthroplasty under spinal anesthesia with limited motor-block.

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Total Knee Arthroplasty
  • Age: Between 50 - 99 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Subjects with chronic knee pain who is indicated for total hip or knee replacement surgery
    2. Subjects who are at least 50 years old
    3. Subjects willing to participate in pre- and postoperative surveys

You may not be eligible for this study if the following are true:

    1. Subjects who failed to complete pre-operative surveys
    2. Subjects with revision Total Knee Arthroplasty
    3. Subjects who had prior ipsilateral knee surgery such as ligament reconstruction or osteotomy
    4. Subjects who had contralateral Total Knee Arthroplasty
    5. Subjects who had prior tibial plateau fracture
    6. Subjects who had ligamentous insufficiency
    7. Subjects with history of fibromyalgia, chronic fatigue syndrome

If you are registered as a volunteer, please login to the dashboard to send referrals.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.