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Role of yavalauha churna in dyslipidemia

To evaluate the efficacy of yavalauha churna in the management of dyslipidemia- An open labeled,randomized controlled clinical trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021369
Enrollment
166
Registered
2019-09-23
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: - Health Condition 2: - Health Condition 3: - Health Condition 4: E789- Disorder of lipoprotein metabolism, unspecified

Interventions

Intervention1: Interventional Yavalauh churan : In interventional,Yavalauh churan is given in the dose of 5gms BD with Madhu for 2 months. Control Intervention1: Comparator agent Tab Atorvastatin: I

Sponsors

SGT University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing for trial is the foremost criteria. 2. Patients having one or more parameters of deranged lipid profile.

Exclusion criteria

Exclusion criteria: 1. Patients having serious ailments like Type 1 DM or poorly controlled Type 2 DM, MI, Cardiac failure, Renal insufficiency, Hypothyroidism, Glucocortico-steroids induced dyslipidemia. 2. Patients on statins/any other drug. 3. The patients more than 40 BMI will not be taken. 4. Pregnant females and lactating mothers.

Design outcomes

Primary

MeasureTime frame
1.Symptomatically, patients will be evaluated as per the scoring pattern. 2.Changes in objective criteria i.e. lipid profile will be analysed and effectiveness of trial drug will be evaluated. 3.normalcy of lipid profile will be the main primary outcome.Timepoint: 1.Symptomatically, patients will be evaluated as per the scoring pattern. 2.Changes in objective criteria i.e. lipid profile will be done on baseline, after 2 months and then one month after completion of the therapy.

Secondary

MeasureTime frame
It is expected that weight and hence, BMI of the patients will be reduced during and after the treatment.Timepoint: BMI will be reduced.

Countries

India

Contacts

Public ContactDr Rekha Phull

SGT University, Gurugram

drrekhasharma99@gmail.com9555953332

Outcome results

None listed

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