跳至主要内容
临床试验/NL-OMON33547
NL-OMON33547已完成3 期

A twenty-six weeks, open-label extension trial to evaluate safety and efficacy of Org 50081 in outpatients with chronic primary insomnia who completed clinical trial protocol 21106 - Extension trial of protocol 21106

Schering-Plough0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • sign written informed consent
  • completed trial 21106 (i.e. completed 26 weeks of treatment and finished the 7-day discontinuation period)

排除标准

  • any (serious) adverse event, medical condition or required concomitant medication deemed relevant for exclusion in trial 21106, as judged by the investigator
  • were significantly non compliant with protocol criteria and procedures of trial 21106, as judged by the investigator

研究者

发起方
Schering-Plough

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