Investigating Patient Satisfaction With Smart Knee Implants

This study is looking at how satisfied patients are with a "smart" knee implant after total knee replacement surgery (total knee arthroplasty, TKA). The smart knee implant helps track your recovery remotely. We want to see if using this smart implant can reduce the number of clinic visits you need after surgery, while still keeping you satisfied and improving your recovery. We're also exploring if your neighborhood's resources affect your recovery, and if your self-reported pain and function match your actual physical improvement. This study is for people aged 18 and older who are having a knee replacement with either the smart implant or standard care. The study status is currently unclear.

Study design
This is an interventional study planning to enroll 150 participants. It compares patients receiving a smart knee implant to those receiving standard-of-care.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your satisfaction and outcomes will be measured from enrollment up to 1 year after your knee replacement surgery.

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NCT06968143

Investigating Patient Satisfaction With Smart Knee Implants

Recruiting
NAAges 18+InterventionalTreatment
University of Chicago
~150 participants
Updated 2025-12-17 on ClinicalTrials.gov
What's tested:Smart Knee Implant

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Patient-Reported Outcomes and Satisfaction
Measured over From enrollment to 1 year after arthroplasty
Total Knee Arthroplasty
Knee Replacement
Knee Replacement Arthroplasty
Knee Osteoarthritis
1 sites across 1 states
Illinois1
  • Sara Wallace, MD · PRINCIPAL_INVESTIGATOR · The University of Chicago Department of Orthopaedic Surgery

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Eligibility criteria

Inclusion

Patients over 18 years of age
Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care

Exclusion

Patients who receive contralateral knee replacement or contralateral or unilateral hip replacement within 90 days before or after their knee replacement in this study
Patients with post-operative weight-bearing restrictions or physical deconditioning prohibiting routine physical therapy participation
  • Patient-Reported Outcomes and SatisfactionFrom enrollment to 1 year after arthroplasty

    The patients in both arms will complete surveys on their subjective pain and function as well as their subjective satisfaction with the knee arthroplasty preparation, surgery, and recovery. The investigators will compare these surveys between the experimental group and the standard-of-care group at select time points.