跳至主要内容
临床试验/EUCTR2007-001611-32-NL
EUCTR2007-001611-32-NL
进行中(未招募)
1 期

A multi-center cardiac safety study of subjects who participated in Organon sponsored Phase 1 and Phase 2 completed and discontinued trials with Org 24448 (Protocols: 22601;22602;22603; 153001;153002;153003;153004, 29402; III.04.0311).

V Organon0 个研究点目标入组 295 人2008年4月29日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
V Organon
入组人数
295
状态
进行中(未招募)
最后更新
6年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2008年4月29日
结束日期
2009年1月1日
最后更新
6年前
研究类型
Interventional clinical trial of medicinal product

研究者

发起方
V Organon

入排标准

入选标准

  • Subjects must:
  • 1\. be verified by the investigator to have participated in a previous Organon sponsored Org 24448 trial
  • 2\. sign an affirmative informed consent before evaluations are conducted;
  • 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

  • Subjects must not have:
  • 1\. have a concurrent acute condition that could interfere the conduct or interpretation of the evaluations. (e.g. acute psychosis, respiratory illness; current experimental medications) if possible evaluation of such subjects is deferred until resolution of such conditions.

结局指标

主要结局

未指定

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