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Post Virechana Ayurvedic Diet for better recovery

To assess the efficacy of Modified Samsarjanakrama with Peyadi Samsarjanakrama in individuals subjected to Virechana. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086585
Enrollment
40
Registered
2025-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: Z684- Body mass index (BMI) 40 or greater, adult Health Condition 2: Z988- Other specified postprocedural states

Interventions

None listed

Sponsors

Dr Nikita Jayappa Koli
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants between 18-60 years of age, Participants who will be fulfilling the, Participants with their prior informed consent for the study, Participants indicated for Peyadi Samsarjana Krama, Participants attained Avara, Madhyama, Pravara Shuddhi lakshana.

Exclusion criteria

Exclusion criteria: Pregnant & Lactating women, Participants indicated for Tarpanadi Samsarjanakrama, Participants indicated for Mamsa rasadi Samsarjanakrama, Participants suffering with Diabetes Mellitus and Hypertension, Participants who attained Heena, Atiyoga lakshana after undergoing Virechana Karma

Design outcomes

Primary

MeasureTime frame
To assess the Agni, adaptability of the taste, modified samsarjanakramaTimepoint: O, 3, 5, 7 days as per the shuddhi lakshana attained by the Participants and later followup after 15 days

Secondary

MeasureTime frame
To assess the Jaranshakti, Abhyavaranashakti, Ruchi, Vata Mutra purusha Mukti before and after the interventionTimepoint: 0,3,5,7 days as per the shuddhi lakshana attained by the Participants and later followup after 15 days

Countries

India

Contacts

Public ContactDr Nikita Jayappa Koli

Alvas Ayurveda Medical College Moodubidire DK Karnataka 574227

drsmithapbhat@gmail.com9480792814

Outcome results

None listed

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