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临床试验/NCT01217879
NCT01217879已完成不适用

Cough Among Hypertensive Patients Treated With Telmisartan, Who Had to Stop Previous ACE-i Treatment Due to Cough

Bayer0 个研究点目标入组 980 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
980
主要终点
Cough frequency among telmisartan treated patients, who had to stop their previous ACE-I treatment due to cough

研究概览

简要总结

In the light of ONTARGET and TRANSCEND studies results, it would be interesting to investigate the real-life telmisartan treatment tolerability. It is well known and accepted that the Real-life setting is much more adequate to reflect the antihypertensive and safety properties of the drug in comparison to the organized and scheduled setting of the clinical trial. Because there are not much data on the cough in relation to telmisartan, therefore it would we worth to observe the cough frequency and general treatment tolerance in patients treated with telmisartan, who had to stop their previous ACE-I treatment due to cough.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hypertension
  • Age > 18
  • ACE-I related cough

排除标准

  • Current treatment with telmisartan
  • Cholestatic disorders and severe hepatic failure
  • Allergy to telmisartan
  • Pregnancy and lactation period

研究组 & 干预措施

Group 1

干预措施: Telmisartan (Kinzal/Pritor, BAY68-9291) (Drug)

结局指标

主要结局

Cough frequency among telmisartan treated patients, who had to stop their previous ACE-I treatment due to cough

时间窗: 4 months after initiation

次要结局

  • Number of Participants with Adverse Events among patients, who had to stop their previous ACE-I treatment due to cough(4 months after initiation)

研究者

发起方
Bayer
申办方类型
Industry

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