To Study the efficacy of agnikarma with suvarna shalaka along with oral administration of dashmooladi kwatha in the treatment of Avabahuka (frozen shoulder)

Phase 3

Not yet recruiting

• Conditions: Adhesive capsulitis of shoulder. Ayurveda Condition: AVABAHUKAH,

• Registration Number: CTRI/2023/11/060119
• Lead Sponsor: Dr Lakshmikant Maheshwarappa Khakre

Brief Summary

This study is a prospective, randomized, open labelled, controlled clinical study of efficacy of agnikarma with suvarna shalaka along with dashmooladi kwath 50ml once a day in evening for one month with follow up and assessment on 1st , 8th, 15th,22nd and 29th day in the treatment of avabahuka with special reference to frozen shoulder. The primary objective is to study the efficacy of suvarna shalaka along with dashmooladi kwath in the treatment of avabahuka with special reference to frozen shoulder.This study is conucted as PG course at a single centre.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-11-18
• Study Start: 2023-12-20

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Selection of patient will be done irrespective of sex, religion, occupation, socio-economic status.
• Patient with classical signs & symptoms of Frozen shoulder with duration up to 2 years.
• Patient between age Group of 40 and 70 years.
• Patients with controlled diabetes mellitus(FBS: <140mg/dl, PPBS:<180mg/dl) with or without medication.
• Patients fit for Agnikarma.

Exclusion Criteria

• Patient with Acute Traumatic Disorders of Shoulder Joints.
• Subluxations or recurrent dislocations of the shoulder joints.
• Patient suffering from arthritis like Osteoarthritis, Gouty arthritis, etc.
• Immunocompromised patients such as HIV, HbsAg & RTPCR positive patients.
• Patients suffering from rotator cuff injuries, other diseases like paralysis, parkinson’s disease, cardiac diseases, renal diseases, endocrine diseases, severe anaemia, malignancy, pregnant & lactating female.
• Patients with uncontrolled diabetes mellitus.(fasting blood sugar (FBS):>140mg/dl, postprandial blood sugar (PPBS):>180mg/dl).

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
improvement in predefined parameters i.e,	28days
Sandhi shoola (pain), Sandhi graha (stiffness), Bahupraspanda Haratvam (Range of Movements) using	28days
goniometer.	28days

Secondary Outcome Measures

Name	Time	Method
1.To achieve relief of pain in Frozen shoulder 2.To evaluate the improvement in the movements of shoulder joint.	28days

Trial Locations

Locations (1)

Government Ayurved Hospital Nanded; 🇮🇳 Nanded, MAHARASHTRA, India

Government Ayurved Hospital Nanded

🇮🇳Nanded, MAHARASHTRA, India

Dr Lakshmikant Maheshwarappa Khakre

Principal investigator

7588178481

lakshmikant.khakre@gmail.com