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临床试验/CTRI/2010/091/000415
CTRI/2010/091/000415已完成2 期

Double-blind, randomised placebo controlled clinical trial to study the add-on efficacy of a standardised preparation of the water extract of Terminalia arjuna in patients with Left Ventricular Dysfunction, already receiving standard drug regimen

Department of Biotechnology Government of India0 个研究点目标入组 100 人开始时间: 待定最近更新:

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

  • Patients (18 years and above) with chronic stable heart failure (stable for three months) with a left ventricular ejection fraction of less than 40 %.

排除标准

  • 1.History of MI or unstable angina within the last 4 weeks.
  • 2.Revascularisation procedures (CABG OR PTCA) done in the past 3 months.
  • 3.Planned for revascularisation in the next three months.
  • 4.Recent stroke or TIA.
  • 5.Uncontrolled hypertension (should be controlled before inclusion)
  • 6.Pregnancy.
  • 7.Other major organ dysfunction.
  • 8.Primary valvular heart disease.
  • 9.Evidence suggestive of ongoing or resolving carditis.
  • 10.Evidence of coarctation of aorta or aortoarteritis.
  • 11.Hypothyroidism

研究者

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