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临床试验/EUCTR2012-001658-24-BG
EUCTR2012-001658-24-BG进行中(未招募)不适用

Efficacy and safety of fixed-dose combination Perindopril 5 mg/ Indapamide 1.25 mg / Amlodipine 5 mg versus Perindopril5 mg / Indapamide 1.25 mg single pill in patients withuncontrolled essential hypertension after 1 month of treatmentby Perindopril 5 mg / Indapamide 1.25 mg single pill withconditional titration based on blood pressure control up toPerindopril 10 mg/ Indapamide 2.5 mg / Amlodipine 10 mg.An international, multicentre, randomised, double blind,4-month superiority study.

Institut de Recherches Internationales Servier0 个研究点目标入组 448 人开始时间: 2013年5月27日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
448

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Men or women of any ethnic origin,
  • - Age = 18 years old or legal national majority,
  • - Confirmed essential uncontrolled hypertension,
  • - Normal or without any clinically significant anomaly 12-lead ECG (left ventricular hypertrophy is authorized at selection and during the study).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 314
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 134

排除标准

  • - Creatinine clearance value classifying them as moderate or severe renal failure
  • - History of hypertension known to be resistant to the free or fixed three-therapy combination with ACE-inhibitors, diuretics and calcium channel inhibitors,
  • - Treatment with more than 2 antihypertensive drugs at the selection visit,
  • - Allergy, hypersensitivity, history of intolerance to indapamide or to any other sulphonamides, to perindopril or any other ACE inhibitor, to amlodipine or any other dihydropyridine, or to any of the excipients,
  • - Congenital galactose intolerance, glucose and galactose malabsorption syndrome, deficit on lactase.

研究者

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