Health Condition 1: null- Rotator cuff Injury
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
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)
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Pain-Visual Analogue ScaleTimepoint: 1 week | — |
Primary
| Measure | Time frame |
|---|---|
| Disabilities of the Arm, Shoulder and HandTimepoint: baseline data before intervention and follow up data after one week. | — |
Countries
India
Contacts
Fr Muller Medical College