跳至主要内容
临床试验/JPRN-jRCT2080223314
JPRN-jRCT2080223314已完成3 期

A double-blind study to assess the efficacy and safety of clazosentan in reducing cerebral vasospasm in patients with aneurysmal subarachnoid hemorrhage treated by endovascular coiling

Idorsia Pharmaceuticals Japan Ltd.0 个研究点目标入组 220 人开始时间: 2016年9月5日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
220

研究概览

简要总结

The incidence of Morbidity/Mortality events was significantly decreased in the clazosentan 10 mg/h group compared with the placebo group. The incidence of adverse events in the clazosentan 10 mg/h group differed from the placebo group in terms of fluid retention events and anemia, but there were no new safety concerns.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 75age old(—)
性别
All

入选标准

  • patients treated by endovascular coiling
  • WFNS GradeI - IV
  • Fisher group 3

排除标准

  • Presence of cerebral vasospasm seen prior to the endovascular coiling etc.

研究者

发起方
Idorsia Pharmaceuticals Japan Ltd.

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