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To study the comparative effect of panchmuli kashaya and meshashrungyadi kashaya with agnikarma in the management of grudhrasi.

A randomized parallel arm comparative clinical study to evaluate the efficacy of panchmuli kashaya and meshshrungyadi kashaya in combination with agnikarma in the management of grudhrasi. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064758
Enrollment
60
Registered
2024-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: G570- Lesion of sciatic nerve Health Condition 2: G570- Lesion of sciatic nerve

Interventions

None listed

Sponsors

Dr Sanjoli Jitendra Waykos
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Participant with classical sign & symptoms of Grudhrasi i.e Ruk Toda, Stambha (at affected right or left leg) 2) Participant between age group of 20-60 years irrespective of religion, occupation and socio-economic status will be selected.

Exclusion criteria

Exclusion criteria: 1) Participant who are suffering from any other known case of systemic diseases i. e. tuberculosis, Cancer, HIV etc. 2) Pregnant and lactating women. 3) Participant taking immunosuppressive medications. 4) Participant with known case of diabetes mellitus will be excluded.

Design outcomes

Primary

MeasureTime frame
To determine effect of Panchmuli Kashaya with Agnikarma in the management of Grudhrasi.Timepoint: 30 days—

Secondary

MeasureTime frame
1)To evaluate the safety of Panchmuli Kashaya with Agnikarma & Meshashrunayadi Kashaya with Agnikarma in the management of Grudhrasi. 2)To understand in detail Samprapti of Grudhrasi.Timepoint: 30th Days—

Countries

India

Contacts

Public ContactDr Sanjoli Jitendra Waykos

seth govindji raoji ayurved mahavidhyalaya solapur

vivek.chandurkar@sgrayurved.edu.in9422788569

Outcome results

None listed

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