Rotator Cuff Tear Clinical Trial
Official title:
Application of a New Polyester Patch in Arthroscopic Massive Rotator Cuff Repair Significantly Improves Clinical Outcome and Tendon Integrity
Verified date | November 2016 |
Source | Etzel Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | Switzerland: Ethikkommission |
Study type | Observational |
The purpose of this study was to assess the impact and potential advantage of a novel synthetic patch augmentation in repair of massive rotator cuff (RC) tears, using clinical and radiological approaches. The investigators hypothesized that implanting this patch will improve individual shoulder function, while reducing re-tear rates compared to the current literature.
Status | Completed |
Enrollment | 54 |
Est. completion date | August 2015 |
Est. primary completion date | August 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 40 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Inclusion criteria were age greater 18 years and a RC tear involving at least two tendons, presenting a massive RC-tear as described by Gerber et al. Exclusion Criteria: - We excluded patients older than 75, fatty infiltration grade 4 according to Goutallier, re-ruptures of former repairs and cases with severe osteoarthritis. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Etzel Clinic |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Function assessed with the Constant-Murley-Score | 25 months | No | |
Primary | Function assessed with the Subjective Shoulder Value | 25 months | No | |
Secondary | Tendon integrity evaluated radiologically | 1-35 months | No |
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