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Comparitive study on Virechana Karma and Basti Karma followed by Vidangadi Churna in the Management of lipid imbalance.

A Clinical Comparative Study on Virechana Karma and Basti Karma followed by Vidangadi Churna in the Management of Medoroga w.s.r. to Dyslipidaemia.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024639
Enrollment
40
Registered
2020-04-15
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: E785- Hyperlipidemia, unspecified

Interventions

Intervention1: Group A â?? 20 patients will be administered Virechana Karma within duration of 15 days as per following plan followed by Vidangadi Churna 3gm twice a day for 30 days. ch.su.23/ 8

Sponsors

National Institute of Ayurveda Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: corticosteroids,antidepressants,anticholinergics, immunosuppressant, oestrogen replacement therapy etc. or any other drugs that may have an influence on the outcome of the study. c)Symptomatic patient with clinical evidence of Heart failure. d)Patients with poorly controlled hypertension (systolic >180 and diastolic >100 mm ofHg) e)Patients with evidence of malignancy. f)Patients on oral contraceptives. g)Alchohol and /or drug abusers. h)Hyper

Exclusion criteria

Exclusion criteria: a)Unstable angina: Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or severe Arrhythmia in the last six months. b)Patients on prolonged ( >6weeks) medication with corticosteroids,antidepressants,anticholinergics, immunosuppressant, oestrogen replacement therapy etc. or any other drugs that may have an influence on the outcome of the study. c)Symptomatic patient with clinical evidence of Heart failure. d)Patients with poorly controlled hypertension (systolic >180 and diastolic >100 mm ofHg) e)Patients with evidence of malignancy. f)Patients on oral contraceptives. g)Alchohol and /or drug abusers. h)Hypersensitivity to any of the trial drugs or their ingredients. i)Patients who have completed participation in any other clinical trial drugs or theiringredients in one month period. j)Patients who have received any cholesterol lowering medication (Modern Drug) within last two weeks. k)Associated with any rectal pathology like haemorrhoids, fissure not fit for Virechanaand Basti Karma etc. l)Pregnancy, Lactation and patients having Dyslipidaemia due to drugs e.g.Glucocorticoids, Diuretics etc. m)Patients having Lipid Profile-Serum Cholesterol >400mg dl, Serum Triglycerides > 400mg/dl, LDL Cholesterol > 250 mg/dl,HDL Cholesterol

Design outcomes

Primary

MeasureTime frame
Changes in lipid profile Change in BMI and BMI Prime. Change in anthropometric parameters Timepoint: Changes in lipid profile - 45 days Change in BMI and BMI Prime. -45 days Change in anthropometric parameters -45 days

Secondary

MeasureTime frame
Reduction in Cardiac risk will be assessed by Framinghms 10 years cardiac risk scoreTimepoint: After completion of trial 45 days

Countries

India

Contacts

Public ContactDr Santvana Sharma

National Institute of Ayurveda Jaipur302002

joshirk1964@gmail.com9414322297

Outcome results

None listed

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