se of various types of Tape in reducing shoulder pain and improve functio
Phase 3
- Conditions
- Health Condition 1: null- Rotator cuff Injury
- Registration Number
- CTRI/2013/07/003847
- Lead Sponsor
- Father Muller Medical Vollege
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Patients who are diagnosed to have rotator cuff injury
Both gender
Age group: 18 to 50 years of age
Reduced Glenohumeral range of motion
Willingness to participate in the trial and signing the informed consent
Exclusion Criteria
Patients who are taking a stable dose of an NSAID and unwilling to undergo a 3-7 days washout period prior to beginning treatment
Currently using immunosuppressive agents or steroidal medications
Currently undergoing any other treatment for the shoulder pain
Undergone any previous shoulder injuries
Referred pain from the cervical spine
Subjects allergic to tape (Zinc oxide)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method