CTRI/2024/05/067265尚未招募3 期
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 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •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.
排除标准
- •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.
研究者
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