CTRI/2024/05/067265Not yet recruitingPhase 3
A Randomised controlled trail to evaluate the efficacy of Ayurveda Intervention (Nitya Virechana)as an add-on to Standard Care in Secondary Hyperlipidemia. - Nil
andini RD0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Patients of all genders between the age group of 20-65 years who fulfil the criteria of Objective and Subjective parameters.
- •2.Controlled HTN -less than or equal to 140/90 mm of Hg.
- •3.Controlled NIDDM -HbA1C less than or equal to 7%.
- •4.Patients fulfilling the diagnostic criteria of Hyperlipidaemia.
- •5.Patients already on Antilipidemic drugs since 0-10years.
- •6.Patients fit for Nitya Virechana.
Exclusion Criteria
- •1.Patients newly diagnosed and not on Antilipidemic drugs.
- •2.Induced Hyperlipidaemia due to prolonged intake of Glucocortiosteriods.
- •3.Patients suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Tuberculosis, Psycho-Neuro-Endocrinal disorders, CKD, Nephrotic Syndrome, Liver disorders etc.)
- •4.Patients with a past history of Atrial Fibrillation, Acute Coronary Syndrome,
- •5.Patient with evidence of malignancy.
- •6.Pregnant and lactating women.
Investigators
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