Actively Recruiting

Phase 4
Age: 50Years - 75Years
All Genders
NCT04975581

Rotator Cuff Tears Repair With or Without Dermal Patch Augmentation

Led by University Hospitals, Leicester · Updated on 2026-05-11

40

Participants Needed

1

Research Sites

264 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The Investigators are planning to conduct a Pilot study of 40 patients of Pragmatic randomised controlled trial comparing rotator cuff tendons repair (small tendons around the shoulder ) with or without augmentative patch. It includes patients between age groups 50 to 75 years with large (≥ 3cm and \< 5 cm ) rotator cuff tear that can be fully repaired using open or mini open repair with or without an augmentation with a human dermal matrix allograft (processed skin graft from a human donor ). The main aim is to examine whether the addition of the patch helps to reduce the rate of re-tear of the rotator cuff tendons at one year following surgery. Patients are randomized to receive either a repair with addition of an augmentative patch or a repair without a patch and have an identical follow-up after surgery. Patients are followed up in outpatient at 6 weeks , 3 months and 12 months after randomization and receive an Magnetic Resonant Imaging (MRI) scan 12 months after surgery. The primary outcome measure is to assess the Re-tear rate of rotator cuff at 12 months after surgery. The secondary outcome measure is to assess functional scores of the shoulder at 12 months . The tertiary outcome measures are to check the cost effectiveness of each procedure.

CONDITIONS

Official Title

Rotator Cuff Tears Repair With or Without Dermal Patch Augmentation

Who Can Participate

Age: 50Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged at least 50 years to 75 years
  • Degenerative cuff tear
  • Large full thickness rotator cuff tear (≥ 3 cm and < 5 cm) that is fully repairable
  • Tears diagnosed using MRI scan
  • Ability to consent
  • Agreement to use of human dermal matrix allograft as augmentative patch
Not Eligible

You will not qualify if you...

  • Previous surgery on the affected shoulder
  • Osteoarthritic changes
  • Unable to have MRI scans
  • Significant neck pathology
  • Cognitive problems or language issue
  • Systemic arthritis
  • Significant dual pathology in the involved shoulder
  • Acute traumatic tears (< 6 months since injury)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University Hopsitals of Leicester NHS Trust

Leicester, United Kingdom

Actively Recruiting

Loading map...

Research Team

U

UHL Sponsor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

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