跳至主要内容
临床试验/EUCTR2008-001875-32-Outside-EU/EEA
EUCTR2008-001875-32-Outside-EU/EEA进行中(未招募)不适用

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study To Evaluate The Efficacy, Safety And Tolerability Of Desvenlafaxine Succinate Sustained-release (DVS SR) In The Treatment Of Children And Adolescent Outpatients With Major Depressive Disorder

Pfizer Inc.0 个研究点目标入组 363 人开始时间: 2016年3月31日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Pfizer Inc.
入组人数
363

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

性别
All

入选标准

  • 1- Age =7 and <18 years of age
  • 2- Primary diagnosis of major depressive disorder (MDD)
  • 3- CDRS-R score >40
  • 4- CGI-S score =4
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 363
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1- History of suicidal behavior, or requires precaution against suicide
  • 2- Not in generally healthy condition
  • 3- History of psychosis or bipolar disorder
  • 4- Seizure disorder

研究者

发起方
Pfizer Inc.

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