CTRI/2024/05/067526CompletedPhase 2/3
A single arm clinical study to evaluate the efficacy of chaturjataka vati in the management of hyperlipidemia
Dr. Amey Rajendra Ekhande1 site in 1 country35 target enrollmentStarted: May 27, 2024Last updated:
Trial Snapshot
- Phase
- Phase 2/3
- Status
- Completed
- Sponsor
- Enrollment
- 35
- Locations
- 1
- Primary Endpoint
- To reduce LDL, Total cholesterol, Triglycerides and Increase HDL levels
Study Overview
Brief Summary
To study the efficacy of Chaturjataka vati in the management of hyperlipidaemia. Total 35 patients will be enrolled. Two tablets of 500 mg will be administered twice a day before food along with the lukewarm water for duration of 60 days and follow up will be done on 20th 40th 60th day and final conclusion will be drawn on the basis of statistical methods.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 30.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age limit from 30 to 70 yrs.
- •Newly detected Hyperlipidemic or known case of Hyperlipidemic patients.
Exclusion Criteria
- •Pregnant women & lactating mothers.
- •Patient with severe renal, hepatic, coronary heart diseases.
Outcomes
Primary Outcomes
To reduce LDL, Total cholesterol, Triglycerides and Increase HDL levels
Time Frame: 60 days study. 20th, 40th, 60th follow up days
Secondary Outcomes
- 1) To study present day food habits and lifestyle as a causative factor for Hyperlipidemia.(2) To study the concept and role of Agnideepana and Amapachana in the management of)
Investigators
Dr Amey Rajendra Ekhande
Dr. D. Y. Patil college of Ayurveda and Research center
Study Sites (1)
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