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A study to know the dose of Achha Snehpana and Pravicharna for bio purification purpose

A comparative study to standardize the dose of Achha Snehpana and Pravicharna for Shodhananga Snehana - Nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066870
Enrollment
40
Registered
2024-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

None listed

Interventions

None listed

Sponsors

Prof Vijay Chaudhary
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group between 18 to 60years. 2. Those who are apparently healthy and fit for Snehana and Shodhana as per classical text.

Exclusion criteria

Exclusion criteria: 1. Individuals below 18 and above 60 years. 2. Those who are contraindicated for Snehana and Shodhana as per classical text. 3. Pregnant women and lactating mothers. 4. Individuals having any chronic ailments like Tuberculosis, Diabetes mellitus, Hypertension, Cardiac disorder or any other chronic illness.

Design outcomes

Primary

MeasureTime frame
Standardization of dose of Achha Snehpana and Pravicharna Snehpana To check for the appearance of Samyak Snigdha Lakshana I.e. Vatanulomna(passage of flatus), Agnidipti(increase in digestive fire), Snigdha Varcha(soft stool), Tvak Snigdhata(softness of skin), Anga Laghava(lightness in body parts), Snehpdvega(disliking of sneha).Timepoint: 2 months—

Secondary

MeasureTime frame
Assessment of health and lipid profile after completion of trial.Timepoint: 2 months—

Countries

India

Contacts

Public ContactSaneha kumari

Rajiv Gandhi Government Postgraduate Ayurvedic College and Hospital Paprola

Charusupriya@gmail.com8894242782

Outcome results

None listed

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