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To see and Compare efficacy of Agnikarma (Heat Therapy),Jalauka Avacharna (Leech Therapy) and Cupping Therapy for Frozen Shoulder

A Triple Arm Open Label Randomized Controlled Comparative Clinical Trial To Evaluate The Efficacy Of Agni Karma, Jalauka Avacharana And Cupping Therapy In The Management Of Avabahuka [Frozen Shoulder - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093297
Enrollment
45
Registered
2025-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M255- Pain in joint

Interventions

None listed

Sponsors

Institute for Ayurved Studies & Research Shri Krishna AYUSH University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having the typical sign and symptoms of Avabahuka and Frozen shoulder between Age group of 30-50 years, of either gender.Patients willing to undergo trial.Patients suffering from controlled Diabetes Mellitus.Patient suitable for Agnikarma. Jalauka Avacharna and Cupping therapy.Patient had signed the consent form.

Exclusion criteria

Exclusion criteria: Age below 30 years and above 50 years,Suffering from specific arthritis like OA, RA etc.,Patients of shoulder joint fracture within last six months,Patients having any surgical procedure on shoulder joint in the last six months,Patients suffering from uncontrolled Diabetes Mellitus and hypertension, and localized skin infection. HIV, Hepatitis, etc. Haematological diseases,Auto Immune disorder like SLE, RA etc.,Pregnant women and lactating mothers, Patient not suitable for Agnikarma, Jalauka Avacharna and Cupping therapy,Patient had not signed the consent form.

Design outcomes

Primary

MeasureTime frame
The Proportion of patient showing improvement in the level of range of motion after trial.Timepoint: 1st- 0 Day 2nd- After completion of Trial 3rd- 2 week after completion of follow up after trial

Secondary

MeasureTime frame
Reduction in the symptoms of patient sandhi shool (pain). Reduction in the symptoms of patient stabadhta (stiffness). Reduction in sandhi shosh. Timepoint: 1st- 0 Day 2nd- After completion of Trial 3rd- 2week after completion of follow up after trial

Countries

India

Contacts

Public ContactDr Naveen Kumar

Institute For Ayurved Studies and Research Shri Krishna AYUSH University

drashishhmehta@gmail.com8950375285

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026