Superior Capsular Reconstruction vs. Partial Repair for Massive Rotator Cuff Tears (NCT03617562)
Arthroscopic Partial Repair vs. Superior Capsular Reconstruction for Massive Irreparable Rotator Cuff Tears: A Pilot Randomized and Controlled Trial
🩺 Plain-English Summary (8th-Grade Level)
Little evidence exists to guide treatment in patients with massive irreparable rotator cuff tears (MRCTS). Arthroscopic partial rotator cuff repair (PRCR) has the longest record of use. The new technique of superior capsular reconstruction (SCR) has more recently been described. Despite high enthusiasm for this technique, its effectiveness, cost and safety profile have not been established. The long-term goal of this study is to perform a multicenter randomized control trial to evaluate the effectiveness of SCR compared to PRCR in patients with MRCTS. The current study is a pilot required to support the development of an expanded formal clinical trial.
Who can join: Review the eligibility criteria below.
Location: Sunnybrook Holland Orthopaedic & Arthritic Centre — Toronto, Ontario
Age range: 18 Years to 65 Years
🧪 Interventions in This Study
- Superior Capsular Reconstruction (PROCEDURE)
- Partial Repair (PROCEDURE)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (2 Sites)
- Sunnybrook Holland Orthopaedic & Arthritic Centre — Toronto, Ontario
- Women's College Hospital — Toronto, Ontario
📞 Contact the Study Coordinator
Phone: (416) 967-8701
Email: patrick.henry@sunnybrook.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Rotator Cuff Tear
- Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears — Phoenix, Arizona
- Stromal Vascular Fraction Cell Therapy to Improve the Repair of Rotator Cuff Tears — New York, New York
- Rotator Cuff Failure With Continuity — Cleveland, Ohio
- FiberLocker® System Augmentation of Rotator Cuff Repairs — Chicago, Illinois
- Decellularized Human Placental Extracellular Matrix Tissue for Rotator Cuff Repair Augmentation — New York, New York
Explore by condition: All Rotator Cuff Tear clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.