CTRI/2009/091/000863已完成3 期
An open label, comparative, multicentric study to assess the efficacy and safety of fixed dose combination capsules of Telmisartan & Indapamide (as sustained release) in comparison with Telmisartan tablets in patients suffering from hypertension
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 200
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 more than or equal to 18 years of age (No upper age limit was mentioned in our Protocol for this clinical trial).
- •2.Patients with hypertension (defined as supine systolic and/or diastolic blood pressure more than 140 mm Hg and 90 mm Hg respectively)
- •3.Informed consent of the patient/relative
排除标准
- •1.Pregnancy and/or Lactation
- •2.Patients with anuria, progressive & severe oliguria, hepatic coma, hypokalaemia, hyponatremia, hypochloremia, volume depletion, hyperuricaemia, secondary hypertension, congestive heart failure, systemic lupus erythematosus.
- •3.Patients with hepatic and /or renal dysfunction or bilateral renal artery stenosis.
- •4.Patients with a history of known hypersensitivity to either Telmisartan or Indapamide or to other sulfonamide derivatives or to any other component of the study drugs
- •5.Patients with any other serious concurrent illness or malignancy
- •6.Patients with continuing history of alcohol and / or drug abuse
- •7.Participation in another clinical trial in the past 3 months
研究者
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