Clin2
NCT04057833Possibly a fitActive, not recruiting

Cell treatment added to rotator cuff repair surgery

Rotator Cuff TearsMuscle Atrophy or WeaknessTendon Rupture - ShoulderSafety Issues

Part of Brain & nervous system, Injuries & trauma clinical trials.

This Phase 1 study tests whether an added cell therapy (E-CEL UVEC cells) can improve healing after arthroscopic (keyhole) rotator cuff repair. It may help people with a specific type of tendon tear who have not improved with standard treatments.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
20 people
Ages
45 years to 70 years
Study type
Interventional

Who can take part

  • You are between 45 and 70 years old
  • Your MRI and exam show a full-thickness supraspinatus tendon tear
  • The tendon has pulled back 1 to 3 cm, and the tendon-fat type score is grade 2 or less
  • You tried non-surgery treatments for at least 3 months (like physical therapy and anti-inflammatory medicines) and they did not help
  • You do not have other shoulder cuff tears besides the supraspinatus tendon
  • You can follow post-surgery rehab and cannot be pregnant

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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