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A clinical trial of single season and all season purgative therapy in healthy individuals with trivrit powder.

A RANDOMIZED COMPARITIVE CLINICAL TRIAL ON SHARADRUTUKALIK TRIVRIT CHURNA AND SARVARUTUKALIK TRIVRIT CHURNA AS A VIRECHAK DRAVYA IN VIRECHANA KARMA FOR THE SWASTHA INDIVIDUAL IN SHARAD RUTU. - VIRECHAN KARMA

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022304
Enrollment
30
Registered
2019-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Group A. Sharada Rutu Kalik Trivrit Churna Virechana: Group A 15 healthy individuals will be treated with Sharada Rutu Kalik Trivrit Churna for Virechana Karma. dose: 24gm each person

Sponsors

Parul Institute of Ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy individuals between age group of 18-60 years of either gender having Madhyama Koshtha. Healthy Individuals who are fit for Virechana. Healthy Individuals who are willing to participate for Virechana Karma.

Exclusion criteria

Exclusion criteria: healthy individuals below 18 and above 60 years of either gender. Individuals who are unfit for Virechana Karma. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Efficacy of Virechana Karma in the context of Shuddhi and Vega.Timepoint: 4 weeks

Secondary

MeasureTime frame
Efficacy of Virechana Karma in the context of Shuddhi, Vega, Purification of bodyTimepoint: 4 weeks

Countries

India

Contacts

Public ContactDr Sangeeta H Toshikhane

Parul Institute of Ayurved

drsangeetaj@gmail.com9964596479

Outcome results

None listed

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