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Arthroscopic Rotator Cuff Repair Utilizing Mechanical Bone Debridement Versus Coblation Debridement — FLOW90  

Rotator Cuff Tears Clinical Trial

Official title:
Arthroscopic Rotator Cuff Repair Utilizing Mechanical Bone Debridement Versus Coblation Debridement: A Prospective Randomized Double Blind Controlled Trial

Clinical Trial Summary

Randomized controlled trial comparing coblation debridement to mechanical debridement in rotator cuff repair.

Clinical Trial Description

Prospective, Double blind, Randomized controlled trial. Male and female subjects, over the age of 18 years. Full thickness rotator cuff tear, requiring surgical repair. Patient undergoes pre- and intra-operative assessment, and once eligibility is confirmed intra-operatively, patient is randomly assigned to receive either a) coblation debridment, or b) mechanical debridement. Standard post-operative rehab program for all patients. Follow-up occurs at 3, 6, 12, and 24 months post operatively and includes physical exam and patient based outcomes (questionnaires). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05084781
Study type Interventional
Source University of Calgary
Contact Ian Lo, MD FRCSC
Phone 403-284-4062
Email ikylo@ucalgary.ca
Status Recruiting
Phase N/A
Start date July 8, 2020
Completion date June 30, 2025
View Details
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