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A Study To Find Out How Well Asitakadichurna Work In Treating Amavata

Randomised Controlled Clinical Trials To Study The Efficacy Of Asitakadichurna In The Management Of Amavata - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099881
Enrollment
60
Registered
2025-12-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

None listed

Sponsors

Dr komal Jivan Parate
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Irrespective of gender and socio-economic status. 2)Patient with sign and symptoms of Amavata like sandhishoola, sandhishoth, sandhistabdhata, sparshasahatva. 3)Known case of Amavata more than 6 week and less than 2 years.

Exclusion criteria

Exclusion criteria: 1)Age below 20 Year and above 60 years. 2)Severe deformities with severe ankylosed joint. 3)Patient who are steroids dependent. 4)Pregnant and lactating mothers. 5)Patient with known case of heart disease DM HTN and other chronic systemic disease. 6)Know case of sandhigata vata and vatarakta.

Design outcomes

Primary

MeasureTime frame
To study efficacy of Asitakadichurna in Amavata by randomised controlled clinical trialTimepoint: Initial assessment at 0 day Follow up after 7th day, 14th day, 21st day Final assessment at 28th day

Secondary

MeasureTime frame
1) To study Amavata in detail as per ayurvedic aspect. 2) To study Asitakadichurna in detail. 3) To compare efficacy of of trial and control drug.Timepoint: Initial assessment at 0 day Follow up after 7th day, 14th day, 21st day Final assessment at 28th day .

Countries

India

Contacts

Public ContactDr Anant Ghare

LRP Ayurvedic Medical College And Hospital PG Institute And Research Center Urun Islampur

dr.anant53@gmail.com9503555535

Outcome results

None listed

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