Prospective Pharmaco-epidemiology Study
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Development of an Ayurvedic informatics database of selected Rasausadhiâ??s in terms of clinical safety.Timepoint: 4 months after recruitment of patients
- Secondary Outcome Measures
Name Time Method Prospective documentation and analysis of information related with prescription trends of selected Rasausadhiâ??s in a structured format to draw the meaningful possible outcomes and conclusions.Timepoint: 4 months after recruitment of patients