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A clinical study of efficacy of sadya virechana karma with eranda payah in management of kaphanubandhi katishoola w.s.r to low back pain

A randomized controlled clinical study to evaluate efficacy of sadya virechana karma with eranda payah In management of kaphanubandhi katishoola with special reference to low back pain

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054216
Enrollment
30
Registered
2023-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: - Health Condition 2: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

None listed

Sponsors

Pramila Vinayak Pawar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Virechana Yogya individuals.43 2) Katishoola more than 15 days and less than 3 months duration (Acute condition). 3) Age of patient 20-45 years. 4) Irrespective of gender and socio-economic status. 5) Any nonspecific condition that may cause low back pain.

Exclusion criteria

Exclusion criteria: 1) Infective spinal disorders. 2) Traumatic condition. 3) Patient having Ano-rectal disorders. 4) Systemic severe illness. 5) Structural vertebral deformities. 6) Person having specific history of heavy labor work or weight lifting for prolong duration

Design outcomes

Primary

MeasureTime frame
To study the effect of Sadya Virechana Karma with Eranda Taila[50ml] and Eranda Payah [100ml] particularly on Kaphanubandhi Katishoola. Timepoint: 1 wk

Secondary

MeasureTime frame
1. To compare effect of Sadya Virechana Karma with Eranda Payah & Dashmool Niruha Basti Once, Twice or thrice in Kaphanubandhi Katishoola. 2. To assess Samyaka Virechana Lakshanas.Timepoint: 1 wk

Countries

India

Contacts

Public ContactM W Nalkande

Government Ayurved College,Nanded

mwnalkande@gmail.com9766694490

Outcome results

None listed

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