CTRI/2020/09/028121招募中2 期
Evaluation of Efficacy and Safety of AYUSH- M3 in the management ofPre-Hypertension â?? A Double blind Randomized control clinical study
CCRAS0 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
- 2 期
- 状态
- 招募中
- 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
- •Patients of either sex aged 30-65 years.
- •Diagnosed patients of Pre hypertension as per 7th report of JNC
- •(120-139 of Hg SBP or 80-89 mm of Hg DBP)
- •Willing and able to participate for 3 months
排除标准
- •Patients who have history of Cardiac Arrhythmia, Acute Coronary Syndrome, Myocardial Infarction, congestive cardiac failure ,Stroke or Severe Arrhythmia in the last 6 months.
- •Essential Hypertension / Secondary hypertension.
- •Patients with concurrent Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction (defined as S. creatinine > 1.2 mg/dl),uncontrolled Pulmonary Dysfunction (asthmatic and COPD patients) or major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Neurological disorders, Endocrinal disorders, etc.) or Known cases of malignancy
- •Uncontrolled Diabetes Mellitus(HbA1C >8)
- •Women who are planning for conception / pregnant or lactating.
- •H/o hypersensitivity to any of the trial drugs or their ingredients.
- •Patient taking participation in any other clinical trial.
- •Any other condition which the P.I. thinks may jeopardize the study.
研究者
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