A Comperative Clinical Study to Evaluate Effecacy of Viddhakarma and Agnikarma in the Management of Avabahuk (Frozen Shoulder)

Phase 2

• Conditions: Health Condition 1: M750- Adhesive capsulitis of shoulderHealth Condition 2: M750- Adhesive capsulitis of shoulder

• Registration Number: CTRI/2023/07/054726
• Lead Sponsor: PGIASR RAU Jodhpur Rajasthan

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Men and women aged 18 years and above.

2. With a new episode of shoulder pain attributable to pain-predominant stage of frozen

shoulder (i.e. within approximately 3 months of onset of symptoms) diagnosed using

criteria set out in the BESS guidelines

3. Who are not being considered for surgery;

4. Willing and able to give informed consent for trial participation and comply with all

study requirements and time line;

Exclusion Criteria

Those with frozen shoulder secondary to significant shoulder trauma (e.g., dislocation,

fracture or full thickness tear requiring surgery) or other causes (e.g. recent breast cancer

surgery or radiotherapy);

2. Those with a neurological disease affecting the shoulder;

3. Those with bilateral concurrent frozen shoulder;

4. Those with other shoulder disorders (e.g., inflammatory arthritis, rotator cuff disorders,

glenohumeral joint instability) or with red flags consistent with the criteria set out in the

BESS guidelines

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement in clinical sign & symptoms of frozen shoulder <br/ ><br>Timepoint: 42 days <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Improvement in quality of lifeTimepoint: 6 week