Connective Tissue Matrix for Rotator Cuff Tendinopathy
Running, not enrolling · Phase 4 · Has a placebo group
Conditions studied: Tendinopathy, Shoulder Pain, Rotator Cuff Tendinitis, Rotator Cuff Tendinosis
In brief
The purpose of this research study is to determine if the effectiveness of a single injection of CTM Boost in the treatment of patients with rotator cuff tendinopathy (RCT) is as effective as a single injection of platelet rich plasma (PRP) in reducing the symptoms of RCT.
Key facts
- Study ID
- NCT06160427
- Run by
- Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
- People needed
- 92
- Starts
- 2023-12-04
- Expected to finish
- 2028-01-15
- Last updated by the study team
- 2025-09-08
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients aged 18-80 years old with rotator cuff tendinopathy
- A PRP or CTM-type injection was determined by the clinician to be the proper medical treatment course and patient is willing to undergo the injection
You may not qualify if…
- Patients with adhesive capsulitis
- Patients with acromio-clavicular joint impingement, retracted tears, significant labral lesions or significant glenohumeral arthrosis
- Patients with joint instability
- History of shoulder surgery or corticosteroid injection in the past 3 months
- Patients with any medical conditions that affect healing, such as end-stage renal disease or uncontrolled diabetes
Where it is running
- Allegheny Health Network Allegheny General Hospital — Pittsburgh, Pennsylvania, United States
- Allegheny Health Network Federal North Medical Office Building — Pittsburgh, Pennsylvania, United States
- AHN Wexford Health & Wellness Pavilion — Wexford, Pennsylvania, United States
- AHN Wexford Hospital — Wexford, Pennsylvania, United States
Full record on ClinicalTrials.gov
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