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

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

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054726
Enrollment
112
Registered
2023-07-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: M750- Adhesive capsulitis of shoulder Health Condition 2: M750- Adhesive capsulitis of shoulder

Interventions

None listed

Sponsors

UPGIASR RAU Jodhpur Rajasthan
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Improvement in clinical sign & symptoms of frozen shoulder Timepoint: 42 days

Secondary

MeasureTime frame
Improvement in quality of lifeTimepoint: 6 week

Countries

India

Contacts

Public ContactDr Upendra Bhardwaj

DrSarwapalli Radakrishnan Rajasthan Ayurved University, Jodhpur

ayurvishnu@gmail.com7742042974

Outcome results

None listed

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