Not Yet RecruitingPhase 4

Rotator Cuff Augmentation With Human Dermal Allograft Versus Bovine Collagen Xenograft Patch: A Randomized Controlled Trial

102 participantsStarted 2024-03

Plain-language summary

Randomized controlled trial comparing human dermal allograft with bovine collagen xenograft in rotator cuff repair.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \>18 years \- fully reparable full thickness rotator cuff tear whereby the treating surgeon feels a graft augment is needed to enhance healing Exclusion Criteria: * tears where only a partial repair is achieved * significant glenohumeral joint arthropathy (Hamada grade 2 and above) * irreparable rotator cuff tears * patients unable or unwilling to consent or comply with study questionnaires * patients with upper limb neurological deficits affecting the ipsilateral limb * workers compensation cases * cases involving litigation

What they're measuring

Western Ontario Rotator Cuff Index (WORC)

Timeframe: 12 mos post-op

Trial details

NCT IDNCT06215417

SponsorUniversity of Calgary

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-09

Contact for this trial

Kristie More, MSc

14032208954 kristie.more@ucalgary.ca

View on ClinicalTrials.gov More Rotator Cuff Tears trials