CTRI/2011/06/001825已完成2 期
CLINICAL STUDY ON HYPERLIPIDEMIA AND COMPARATIVE EVALUATION OF EFFICACY OF A COMPOUND UNANI FORMULATION (SAFOOF-E-MUAHAZZIL) AND COMPRESSED TABLET OF SAFOOF-E-MUHAZZIL IN ITS MANAGEMENT
Department of Moalejat Medicine Faculty of Medicine1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2010年5月24日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- hyperlipidemia
研究概览
简要总结
The purpose of this study is to evaluate the comparative effect of a compound Unani formulation (Safoof-e-Muhazzil) and compressed tablet of same drug i.e., Safoof-e-Muhazzil in hyperlipidemia against a standard control i.e, Atorvastatin and to establish their tolerability and efficacy. Serum cholesterol, VLDL, LDL, HDL, and Triglycerides together with BMI, Waist To Hip Ratio and Blood Pressure will be used to compare the status of Blood Lipids,obesity and Hypertension before and after treatment, and scored to determine the efficacy of the treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Open Label
入排标准
- 年龄范围
- 20.00 Year(s) 至 70.00 Year(s)(—)
- 性别
- All
入选标准
- •Person aged
- •70 Years M/F Patients willing to sign consent form & participate in Clinical Trial voluntarily. Hyperlipidemic.
排除标准
- •Persons below 20 yrs and Above 70 yrs of age Pregnancy Liver diseases Renal diseases Diabetes mellitus Type II Alcoholic AIDS Thyroid Disease Drug intake ?
- •Corticosteroids, Diuretics, Beta-blockers, Oral contraceptives, Cyclosporin, Androgens & Retinoids.
结局指标
主要结局
hyperlipidemia
时间窗: 0,2,4, and 6 weeks
次要结局
- obesity, hypertension(0,2,4, and 6 weeks)
研究者
研究点 (1)
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