Actively Recruiting
REST-Knee: A Pilot RCT of 72-Hour Knee Immobilization and Pain Outcomes
Led by Université de Sherbrooke · Updated on 2026-04-06
106
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Postoperative pain following total knee arthroplasty (TKA) is often difficult to manage, particularly with the increasing use of outpatient surgery where patients recover at home. This study aims to evaluate whether wearing a knee extension brace for the first 72 hours after surgery can reduce pain and improve recovery. This pilot randomized controlled trial will compare two groups of patients undergoing primary unilateral TKA: one group will wear an extension brace continuously for 72 hours after surgery, while the control group will follow standard care with early mobilization. Participants will be followed for up to 12 months. The primary objective of this pilot study is to assess the feasibility of conducting a larger trial, including recruitment rates, adherence to the intervention, follow-up completion, safety, and acceptability. Clinical outcomes will also be explored, including pain at 2 and 6 weeks after surgery (measured using a visual analog scale), knee function, range of motion, opioid consumption, complications, healthcare use, and quality of life. The study hypothesizes that short-term immobilization of the knee in full extension will reduce postoperative pain and may improve early recovery outcomes. Findings from this pilot study will inform the design of a larger definitive trial and may contribute to improving postoperative care and pain management after knee replacement surgery.
CONDITIONS
Official Title
REST-Knee: A Pilot RCT of 72-Hour Knee Immobilization and Pain Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults undergoing primary unilateral total knee arthroplasty for knee osteoarthritis at CHUS
You will not qualify if you...
- Known thrombophilia or bleeding disorders
- History of thromboembolic events
- Contraindications to brace use such as material allergy
- Revision or constrained knee prostheses
- Use of continuous postoperative nerve block infusion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CIUSSS de l'Estrie-CHUS, 3001, 12e Ave Nord, Sherbrooke, Qc, Canada, J1H 5N4
Sherbrooke, Quebec, Canada, J1K 2P2
Actively Recruiting
Research Team
S
Sonia Bedard, Masters
CONTACT
Y
Yoan Bourgeault-Gagnon, MD FRCSC
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here