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Study identifier: NCT04975581 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Rotator Cuff Tears Repair With or Without Dermal Patch Augmentation

Condition: Rotator Cuff Tears  ·  Sponsor: University Hospitals, Leicester

PhasePhase 4
Planned participants40
Who can joinAll sexes, 50 Years to 75 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

UHL Sponsor  ·  +44 116 258 8239 (1823)  ·  uhlsponsor@uhl-tr.nhs.uk

Always discuss trial participation with your own doctor first.

Locations (1)

University Hopsitals of Leicester NHS TrustLeicester, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT04975581