Intervention with Murivenna bandage in acute rotator cuff injury in reducing pain and improving abduction in selected participants
Not Applicable
- Conditions
- Health Condition 1: S460- Injury of muscle(s) and tendon(s)of the rotator cuff of shoulderHealth Condition 2: S460- Injury of muscle(s) and tendon(s)of the rotator cuff of shoulder
- Registration Number
- CTRI/2024/07/070636
- Lead Sponsor
- DrAmrutha S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Participants Diagnosed As Acute Rotator Cuff Injuries With U.S.G Or M.R.I
Participants Within Age Group 30-60 Years Old
Participants With Informed Written Consent
Exclusion Criteria
Participants With History Of Pulmonary Tuberculosis, Muscle Wasting And Congenital Joint Disorders.
Participants Associated With Fracture In And Around The Shoulder.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Evaluate The Effect Of Murivenna Bandage In Reducing Pain And Improving Abduction In Acute Rotator Cuff InjuryTimepoint: Pain and abduction will be assessed in 0th,7th,14th,21st and 28th day
- Secondary Outcome Measures
Name Time Method To Evaluate The Study Of Murivenna Bandage In Improving Quality Of Life Assessed Using Shoulder Pain And Disability Inedx (SPADI)Timepoint: 0TH,7TH,14TH,21ST And 28TH Days