跳至主要内容
临床试验/NCT00225511
NCT00225511已完成3 期

Phase III Multi-Center, Double-Blind, Comparative Study of Effexor XR for the Treatment of Depression

Wyeth is now a wholly owned subsidiary of Pfizer73 个研究点 分布在 1 个国家目标入组 590 人开始时间: 2004年6月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
590
试验地点
73
主要终点
Response rate of HAM-D17 (Hamilton Rating Scale for Depression) at the final-on-therapy.

研究概览

简要总结

Study Evaluating Effexor XR for Major Depression.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
20 Years 至 64 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients diagnosed with major depression based on DSM-IV-TR
  • •Patients having minimal total score of 18 on the HAM-D17 and minimal score of 2 on the item of "depressed mood" at the baseline.

排除标准

  • •Patients with schizophrenia or any other psychotic disorder
  • •Patients with history or presence of bipolar disorder

结局指标

主要结局

Response rate of HAM-D17 (Hamilton Rating Scale for Depression) at the final-on-therapy.

次要结局

  • Difference of total score of HAM-D17 between baseline and final-on-therapy.
  • Remission rate of HAM-D17 at the final-on-therapy.

研究者

发起方
Wyeth is now a wholly owned subsidiary of Pfizer
申办方类型
Industry

研究点 (73)

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