Evaluating the effectiveness of vitamin C intake in patients diagnosed with rotator cuff tears undergoing arthroscopic treatment
Phase 3
Recruiting
- Conditions
- Rotator Cuff tear.
- Registration Number
- IRCT20231021059783N1
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 131
Inclusion Criteria
All paitents undergoing arthroscopic treatment due to rotator cuff tendon tear in year 1402- 1403 after having signed the consent form will enter the study
Exclusion Criteria
A retraction of at least one tendon superior or equal to grade 3
Fatty degeneration of at least one muscle superior or equal to grade 3
An anatomically non-repairable tear
An isolated injury of the subscapular tendon
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Pre operation, 6 months post-operation. Method of measurement: Yes-No questions based on American Shoulder and Elbow Surgeons questionare and Visual Analogue Scale.;Rotator Cuff tendon range of motion. Timepoint: Pre operation, 45 days post-operation, 3 months post-operation, 6 months post-operation. Method of measurement: Based on American Shoulder and Elbow Surgeons questionare and Goniometry.
- Secondary Outcome Measures
Name Time Method