跳至主要内容
临床试验/EUCTR2005-001135-30-IT
EUCTR2005-001135-30-IT进行中(未招募)1 期

A multi-center, randomized, parellel group, comparative, active controlled, safety-assessor blinded, phase IIIa, pivotal trial, in adult subjects comparing Org 25969 with neostigmine as reversal agent of a neuromuscolar block induced by rocuronium or vecuronium at reappearance of T2

ORGANON ITALIA0 个研究点目标入组 196 人开始时间: 2005年10月26日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
196

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

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
ORGANON ITALIA

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