To Study the Effect of a Blood Product named Platelet Rich Plasma in Shoulder Tendon Injuries .
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062451
- Lead Sponsor
- DMIHER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age 18-60 years,
Patients of Partial or Complete Rotator Cuff Tear ,
Primary , Degenerative or Traumatic Rotator Cuff Injuries
Exclusion Criteria
History of shoulder fracture involving humeral head on affected side
Previous Operative Intervention of the Ipsilateral Shoulder
Rotator Cuff Tear associated with other pathologies
Previous infection in the same shoulder
Uncontrolled Diabetes
Patients with Bleeding tendencies and
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method