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To study efficacy of 5ml castor oil with 50ml dry ginger decoction in the management of lower back pain with special reference to Chakradatta

Randomised clinical trial to study efficacy of Eranda Sneha(5ml)with Shunthi Kwatha(50ml) in the management of Katishoola with special reference to Chakradatta.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046583
Enrollment
35
Registered
2022-10-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system Health Condition 2: M958- Other specified acquired deformities of musculoskeletal system

Interventions

None listed

Sponsors

Sane Guruji Arogya Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having symptom of Katishool more than 7 days and less than 3 months. 2. Avarodha Janya Samprapti. 3. No specific and major pathology of degenerative changes 4. Gender - Male and Female

Exclusion criteria

Exclusion criteria: 1.Taking NSAIDs 2.Patient having inborn structural deformities. 3. Diagnosed with Fracture of Lumbar Spine etc. and needs surgical intervention 4.Patients having other joint deformities or diseases which are not related to Katishoola. 5. Katishoola is associated with known case of Cardiac disease, Pulmonary TB, Pregnancy, Paralysis, Neurological disorder, HIV or any other relevant pathology.

Design outcomes

Primary

MeasureTime frame
Primary outcome is assessment of Katishoola with pain scaleTimepoint: intervention for consecutive 7 days

Secondary

MeasureTime frame
Comparative analysis of pain and functional improvement Timepoint: Day 1 and Day 7 2visit

Countries

India

Contacts

Public ContactDr Simaran Gani Mulla

MAMs Sumatibhai Shah Ayurved Mahavidyalaya, Pune

prof.dr.nileshkulkarni@gmail.com8805335512

Outcome results

None listed

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