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Study of effect of Gomutradi Kshara in Medoroga (dyslipidaemia)

Preclinical and Clinical Evaluation of Gomutradi Kshara in the Management of Medoroga With Special Reference to Dyslipidaemia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/04/018826
Enrollment
30
Registered
2019-04-29
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: Gomutradi Kshara: Gomutradi Kshara in dose of 1 capsule (500 mg) thrice in a day with lukewarm water for 30 days. Control Intervention1: Tablet Shuddha Guggulu (Commiphora Mukul) (Ext

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between the age group of 18-60 years of either sex. 2. Diagnosed & confirmed cases of Dyslipidaemia ( Medoroga) on the basis of criteria given by NCEP-ATPIII. (If any one of the following) a) Serum Cholesterol >= 200 mg/dl b) Serum Triglycerides >= 150 mg/dl c) LDL Cholesterol >= 130 mg/dl d) HDL Cholesterol 3. Willing and able to participate in the study for 1 months.

Exclusion criteria

Exclusion criteria: 1. Patients having medical history of- a) Unstable angina b) Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or severe Arrhythmia in the last six months. c) Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants, anticholinergics, immunosuppressants, oestrogen replacement therapy etc. or any other drugs that may have an influence on the outcome of the study. d) Symptomatic patient with clinical evidence of Heart failure. e) Patients with poorly controlled hypertension (systolic >160 and diastolic >100 mm of Hg) f) Uncontrolled Diabetes Mellitus. g) Impaired Renal function (Creatinine >2mg/dl). h) ALT and AST > 2 times of upper limit of normal (40 mg/dl). i) Hypothyroidism. j) Patients with evidence of malignancy. k) Patients on oral contraceptives. l) Alcoholics and /or drug abusers. m) Hypersensitivity to any of the trial drugs or their ingredients. n) Patients who have completed participation in any other clinical trial drugs or their ingredients. o) Patients who have received any cholesterol lowering medication (Modern Drug within last two weeks. 2. Pregnancy, Lactation and patients having Dyslipidaemia due to drugs e.g. Glucocorticoids ,Diuretics etc.

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of Medoroga (Dyslipidaemia)Timepoint: Assessment on 15th and on completion of trial i.e. on 31st day

Secondary

MeasureTime frame
1 Improvement in lipid profile 2 comparison of effect of Gomutradi Kshara and Suddha Guggulu (extract) in Medoroga (Dyslipidaemia).Timepoint: Assessment on baseline and after completion of trial i.e. on 31st day.

Countries

India

Contacts

Public ContactDr Rama Kaswan

National Institute of Ayurveda

ursarojayu@gmail.com9983341119

Outcome results

None listed

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