To study management of chaturjatak vati in hyperlipidemia

A single arm clinical study to evaluate the efficacy of chaturjataka vati in the management of hyperlipidemia - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067526

Enrollment

Registered

2024-05-17

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age limit from 30 to 70 yrs. 2) Newly detected Hyperlipidemic or known case of Hyperlipidemic patients.

Exclusion criteria

Exclusion criteria: 1) Pregnant women & lactating mothers. 2) Patient with severe renal, hepatic, coronary heart diseases.

Design outcomes

Primary

Measure	Time frame
To reduce LDL, Total cholesterol, Triglycerides and Increase HDL levelsTimepoint: 60 days study. 20th, 40th, 60th follow up days	—

Secondary

Measure	Time frame
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 hyperlipidemia.Timepoint: 60 days study. 20th, 40th, 60th follow up days	—

Countries

India

Contacts

Public ContactDr Gunvant Yeola

Dr. D. Y. Patil college of Ayurveda and Research center

Gunvantayurved@gmail.com9028321955

Outcome results