CTRI/2020/09/027526尚未招募2 期
A prospective open labeled observational study to document the potential safety issues and prescription trends of selected Rasausadhiâ??s in CCRAS -OPDâ??s across India - Pharmaco-epidemiological Study
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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 who have normal levels of liver and kidney function tests.
- •2. Patients willing to participate in the study for a minimum period of 1week to a maximum of 6 weeks.
排除标准
- •1. Presence of renal or hepatic dysfunction.
- •2. Subjects who have a history of Cardiac Arrhythmia, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia, Carcinoma etc
- •3. Subjects with uncontrolled Pulmonary Dysfunction (asthmatic and COPD patients) or other concurrent severe disease.
- •4. Uncontrolled Diabetes Mellitus (HbA1C >8)
- •5. Any concurrent condition (medical, social or behavioral) that, in the opinion of the research team, would preclude or confound acquisition or interpretation of data or delivery of care.
- •6. Patient having the H/O intake of Rasaoushadhi in the past 6 weeks.
研究者
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