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EFFICACY OF VIRECHANA AND UDWARTANA KARMA IN THE MANAGEMENT OF STHAULYA (OBESITY)

EFFICACY OF VIRECHANA KARMA AND UDWARTANA KARMA IN THE MANAGEMENT OF STHAULYA (OBESITY) AN OPEN LABELED RANDOMIZED COMPARATIVE CLINICAL TRIAL - VUS

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032623
Enrollment
30
Registered
2021-04-07
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

Health Condition 1: E669- Obesity, unspecified

Interventions

Intervention1: Virechana Karma: Virechana will be done by Ichhabhedi Rasa - (4-6 tablet, each tablet 125mg) Anupana: Sharkara Yukta Jala (10gm Sharkara + 200 ml water) At Shleshma Kale Gate Intervent

Sponsors

Government Akhandanand Ayurved Mahavidyalaya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients between the age group of 18 to 60 years with classical signs and symptoms of Sthaulya. Patients having BMI (Body Mass Index) greater and equal to 25 and less than equal to 35 will be taken for the study. In Shodhana group Virechana Yogya as per Ayurvedic Classic will be included.

Exclusion criteria

Exclusion criteria: Patients having age less than 18 and greater than 60 will be excluded. Known case of serious Cardiac, Renal or Hepatic diseases, Hypertension, AIDS, STD, TB etc. Obesity due to drugs e.g. Anticonvulsant, Antipsychotics, Beta-blockers etc. Pregnant and lactating women. BMI: less than 25 and greater than 35 will be excluded. In Shodhana group Virechana Ayogya as per Ayurvedic Classics will be excluded

Design outcomes

Primary

MeasureTime frame
To reduce weight gain (obesity) in the patientsTimepoint: 21 days

Secondary

MeasureTime frame
To improve quality of life of obesity patientsTimepoint: 35 days

Countries

India

Contacts

Public ContactUrvashi Patel

Government Akhandanand Ayurved Mahavidyalaya

vdfalgun@gmail.com8320889714

Outcome results

None listed

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