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effect of Shuddha Shyama Trivrit dose in Virechana Karma according to Koshtha

A Randomized Clinical Study to Validate the Classical Dose of Shuddha Shyama Trivrit in Virechana Karma as per Koshtha Assessment - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106165
Enrollment
30
Registered
2026-03-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

RGGPG Ayurvedic College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a)Volunteers with Age group between 18 to 50 years. b) Individuals who are apparently healthy, individuals fit for Virechana Karma as per classical text. c) Individuals willing to provide written informed consent for participation in the study.

Exclusion criteria

Exclusion criteria: a)Individuals contraindicated for Virechana Karma per classical text. b)Individuals who have undergone any Panchkarma therapy (i.e. Vamana, Virechana, Basti and Nasya) recently. c)Pregnant women and lactating mothers. d)Individuals with Hb less than 10gm/dl and electrolytes imbalances. e)Individuals with history of Chronic Gastrointestinal disorders, Metabolic disorders Diabetes Mellitus & Hypertension etc.

Design outcomes

Primary

MeasureTime frame
a)To evaluate the subjective and objective response of Virechana Karma based on Koshtha.Timepoint: 18 days

Secondary

MeasureTime frame
a) To analyze biochemical and physiological changes (eg. Electrolytes balance, hydration status) after undergoing Virechana Karma. b) To observe pharmacological action of Shuddha Shyama Trivrit in the context of Virechana Karma.Timepoint: 18days

Countries

India

Contacts

Public ContactDr Monika

Rajiv Gandhi Government Post Graduate Ayurvedic College and Hospital paprola Distt. Kangra HP

anil5karma@gmail.com9418466766

Outcome results

None listed

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