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Intervention with Murivenna bandage in acute rotator cuff injury in reducing pain and improving abduction in selected participants

Effect Of Murivenna Bandage In Acute Rotator Cuff Injury - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070636
Enrollment
36
Registered
2024-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: S460- Injury of muscle(s) and tendon(s)of the rotator cuff of shoulder Health Condition 2: S460- Injury of muscle(s) and tendon(s)of the rotator cuff of shoulder

Interventions

None listed

Sponsors

DrAmrutha S
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: Participants With History Of Pulmonary Tuberculosis, Muscle Wasting And Congenital Joint Disorders. Participants Associated With Fracture In And Around The Shoulder.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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—

Countries

India

Contacts

Public ContactDr M M Abdul Shukkoor

Govt. Ayurveda College Tripunithura Ernakulam

drsukoor@gmail.com7034705947

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026