跳至主要内容
临床试验/EUCTR2004-000240-25-IT
EUCTR2004-000240-25-IT进行中(未招募)不适用

An 8 week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study toevaluate the efficacy and safety of aliskiren administered alone and in combination with hydrochlorothiazide inpatients with essential hypertension.

OVARTIS FARMA0 个研究点目标入组 2,685 人开始时间: 2005年5月17日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
OVARTIS FARMA
入组人数
2,685

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

  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

发起方
OVARTIS FARMA

相似试验

进行中(未招募)
不适用
An 8 week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with hydrochlorothiazide in patiens with essential hypertensio
EUCTR2004-000240-25-SEovartis Sverige AB2,685
进行中(未招募)
1 期
An 8 week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with hydrochlorothiazide in patiens with essential hypertensio
EUCTR2004-000240-25-SKovartis s.r.o.
进行中(未招募)
不适用
An 8-week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with amlodipine in patients with essential hypertension.hypertension
EUCTR2008-001609-40-DKovartis Pharma Services AG1,611
进行中(未招募)
不适用
An 8-week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with amlodipine in patients with essential hypertension.hypertension
EUCTR2008-001609-40-GRovartis Pharma Services AG1,611
进行中(未招募)
不适用
An 8-week double-blind, multicenter, randomized, multifactorial, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren administered alone and in combination with amlodipine in patients with essential hypertension.MedDRA version: 9.1Level: LLTClassification code 10020772Term: Hypertensionhypertension
EUCTR2008-001609-40-FIovartis Pharma Services AG1,611