CTRI/2014/07/004804已完成2 期
A two arm randomized, open labeled, prospective, multi-centre, clinical study to evaluate efficacy and safety of Dabur Ratnaprash in health & immunity related parameters
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 100
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
- •Male and female subjects aged 18 to 60 years (both the ages inclusive)
- •Ready to provide written informed consent
- •No history of any known allergy with Chyawanprash like products or any of the ingredientts of the Ratnaprash
- •Willing to come for the follow up visits for evaluation
排除标准
- •Presence of clinically significant abnormal laboratory, ECG or X-ray findings during screening.
- •Patients with known uncontrolled diabetes mellitus (DM), hypertension (HT), symptomatic congestive heart failure (CHF), unstable angina pectoris, myocardial infarction (MI)
- •Patients participated in another clinical drug trial within 3 months before recruitment in this trial
- •Any other medical condition that in the Investigators opinion would preclude patient participation
- •Pregnant and breast feeding women and women of child bearing age refusing to use contraceptive measures
- •Immunologically compromised individuals
研究者
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