CTRI/2021/12/038589招募中3 期
Prospective Double blind Randomized controlled clinical study on Ayurvedic intervention (Sarpgandha Mishran) vs Amlodipine for the management of stage-I Primary Hypertension
试验速览
- 阶段
- 3 期
- 状态
- 招募中
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 of either sex aged 30-65 years
- •2.Diagnosed patients of stage-I essential hypertension as per 8th report of JNC (140-159 mm of Hg SBP and 90-99 mm of Hg DBP)
- •3.Willing and able to participate for 3 months
排除标准
- •1.Patients who have history of Myocardial Infarction, congestive cardiac failure, Stroke or Arrhythmia in the last 6 months.
- •2.Secondary hypertension.
- •3.Patients with concurrent Hepatic Dysfunction (defined as AST and/or ALT > 3 times of the upper normal limit) or Renal Dysfunction (defined as S. creatinine > 1.4 mg/dl),uncontrolled Pulmonary Dysfunction (asthmatic and COPD patients) or major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Neurological disorders, endocrine disorders, etc.) or known cases of malignancy.
- •4.Known cases of uncontrolled Diabetes Mellitus.
- •5.Women who are planning for conception / pregnant or lactating.
- •6.Patients suffering from Psychosis/depressive illness.
- •7.H/o hypersensitivity to any of the trial drugs or their ingredients.
- •8.Patient taking participation in any other clinical trial.
- •9.Participants who were tested COVID-19 positive (through a positive RT-PCR) in the last 30days.
- •10.Participants with Post COVID-19 complications or BP fluctuations following disease.
- •11.Participants who are still on COVID-19 related medical interventions.
- •12.Any other condition, which the P.I. thinks, may jeopardize the safety of the patients.
研究者
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