Investigating Patient Satisfaction With Smart Knee Implants
University of Chicago · NCT06968143
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 150
- US sites recruiting
- 1
- Study start
- September 1, 2025
- Record last updated
- December 17, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The main goal of this study is to see if there is a connection between the social and economic resources available in a patient's neighborhood (measured by the Area Deprivation Index, ADI) and their recovery after knee replacement surgery, as tracked through remote monitoring. A secondary goal is to find out if patients' self-reported pain and function score are linked to their actual physical improvement after surgery as measured by a remote therapeutic monitoring (RTM) device. Additionally, this study examines whether RTM can reduce the number of postoperative clinic visits within the first 90 days after surgery while maintaining patient satisfaction and patient-reported outcome measures (PROMs).
Being studied: Smart Knee Implant
Conditions: Total Knee Arthroplasty; Knee Replacement; Knee Replacement Arthroplasty; Knee Osteoarthritis
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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 Criteria
- 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
Recruiting US locations
The University of Chicago Medical Center
Chicago, IL 60637
Site contact: Sara Wallace, MD · 773-834-3531 · swallace2@bsd.uchicago.edu
Study contacts (from the official record)
- Malik J Scott, BA · 773-834-0822 · mjscott1@uchicago.edu
- Vincent Buckman, BS · vincent.buckman@uchicagomedicine.org
Similar studies in Illinois
All arthritis studies in Illinois →- RecruitingPhase 2
A Clinical Study of Tulisokibart (MK-7240) to Treat Radiographic Axial Spondyloarthritis (MK-7240-013)
Merck Sharp & Dohme LLC
- Location
- Chicago, IL + 35 other US sites
- Eligibility basics
- Ages 18–80
- RecruitingPhase 3
Phase 3 Pivotal Trial Comparing CARTISTEM® and Surgical Comparator for Knee Cartilage Lesions and Osteoarthritis
Medipost, Inc.
- Location
- Chicago, IL + 33 other US sites
- Eligibility basics
- Ages 18–75
- RecruitingPhase 1
A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effectiveness of Intravenous Infusions and Subcutaneous Injections of ABBV-519 in Adult Participants With Systemic Lupus Erythematosus (SLE) or…
AbbVie
- Location
- Orland Park, IL + 11 other US sites
- Eligibility basics
- Ages 18–75
- RecruitingPhase 3
A Double-blind, Randomized Controlled Trial to Investigate the Efficacy, Safety, and Pharmacokinetics of Pegloticase Administration Via Subcutaneous and Intravenous Routes Both With Methotrexate in Participants With…
Amgen
- Location
- Chicago, IL + 73 other US sites
- Eligibility basics
- Ages 18+