Rotator Cuff tear.
Conditions
Interventions
Intervention 1: Intervention group: Vitamin C + group in which they recieve vitamin c supplement 500mg per day, oral, for 45 days. Intervention 2: Control group: Vitamin C - group in which they wont r
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactGhazal Ejlali
Kerman University of Medical Sciences
Outcome results
None listed