examining of the effect of PRP on improving shoulder functio
Not Applicable
- Conditions
- Tendonopathy.Injury, poisoning and certain other consequences of external causes
- Registration Number
- IRCT20230610058440N1
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
All patients between the ages of 18 and 65 who have shoulder pain during activity and a pain score greater than 5.10
Exclusion Criteria
The presence of another cause other than tendon disorders in the shoulder axis
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Shoulder function score in the Munich questionnaire. Timepoint: At the beginning of the study and 3 and 6 months after PRP injection. Method of measurement: Munich questionnaire.
- Secondary Outcome Measures
Name Time Method