Decellularized Human Placental Extracellular Matrix Tissue for Rotator Cuff Repair Augmentation (NCT07027735)
๐ฉบ Plain-English Summary (8th-Grade Level)
The rotator cuff is a set of muscles and tendons that help move the shoulder. Tears in the rotator cuff are common, particularly as people age. Consequently, rotator cuff repair surgeries are common, as well. Despite the frequency with which rotator cuff repairs are performed, there remains a high rate of postoperative failure to heal. In such situations, there is a lack of connective tissue establishment between the rotator cuff tendon and the bone. One strategy to attempt to improve healing of the rotator cuff tendon back to the bone is via the use of extracellular matrix allograft. This treatment is composed of tissue from other humans, which is stripped of its cells so that just the scaffolding around the cells remains. This decellularized scaffolding can be placed at the rotator cuff healing site in an attempt to augment healing. Both animal studies and human studies have shown promise with this approach. Of those patients enrolling in the study, 50% will be assigned at random to receive a standard rotator cuff repair AND allograft treatment, while 50% will be assigned at random to receive standard rotator cuff repair WITHOUT allograft treatment. All patients enrolled in the study will also obtain an MRI at one year following surgery in order to assess tendon healing. Of note, one-year postoperative MRIs are not standard following rotator cuff repair - only those enrolled in the study will receive this MRI. There will be no financial consequence of receiving this MRI.
Who can join: Review the eligibility criteria below.
Location: NewYorkPresbyterian Hospital @ Columbia โ New York, New York
Age range: 18 Years
๐งช Interventions in This Study
- Rotator Cuff Repair with Allograft Patch (OTHER)
- Rotator Cuff Repair with No Augmentation (OTHER)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- NewYorkPresbyterian Hospital @ Columbia โ New York, New York
๐ Contact the Study Coordinator
Phone: (860) 459-5700
Email: al3896@cumc.columbia.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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 ยง 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 โ Phoenix, Arizona
- Stromal Vascular Fraction Cell Therapy to Improve the Repair of Rotator Cuff Tears โ New York, New York
- Rotator Cuff Failure With Continuity โ Cleveland, Ohio
- FiberLockerยฎ System Augmentation of Rotator Cuff Repairs โ Chicago, Illinois
- Superior Capsular Reconstruction vs. Partial Repair for Massive Rotator Cuff Tears โ Toronto, Ontario
Explore by condition: All Rotator Cuff Tear clinical trials
๐ก 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.