跳至主要内容
临床试验/NCT00534599
NCT00534599已完成3 期

A Multicenter, Rand., Double-blind, Parallel-group, Pbo-controlled Study of the Efficacy and Safety of SEROQUEL® XR Compared With Pbo as an Adjunct to Treatment in Patients With Generalized Anxiety Disorder Who Demonstrate Partial or No Response to a SSRI or SNRI Alone or in Combination With a Benzo

AstraZeneca1 个研究点 分布在 1 个国家目标入组 409 人开始时间: 2007年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
AstraZeneca
入组人数
409
试验地点
1
主要终点
Least Square Mean Change From Randomization to Week 8 in Hamilton Rating Scale for Anxiety (HAM-A) Total Score

研究概览

简要总结

This study is being carried out to see if extended release quetiapine fumarate (Seroquel®XL) when added to standard selective serotonin reuptake inhibitor (SSRI) / serotonin-norepinephrine reuptake inhibitor (SNRI) therapy is effective and safe for the treatment of Generalized Anxiety Disorder in patients with partial or no response to SSRI/SNRI alone or in combination with a benzodiazepine, and if so, how it compares with placebo

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Provision of Informed Consent
  • Documented diagnosis of Generalized Anxiety Disorder
  • Female patients must not be pregnant and be willing to use a reliable method of birth control
  • Be able to understand and comply with study requirements

排除标准

  • Other psychiatric disorders that could confound the study results, as judged by the study doctor
  • Moderate to severe depression
  • Other clinically relevant diseases, as judged by the study doctor
  • Medication that you are taking, as judged by the study doctor

研究组 & 干预措施

1

Other

Adjunctive Placebo Seroquel XR to anxiety treatment

干预措施: Placebo (Drug)

2

Experimental

Adjunctive Seroquel XR to anxiety treatment

干预措施: quetiapine fumarate XR (Drug)

结局指标

主要结局

Least Square Mean Change From Randomization to Week 8 in Hamilton Rating Scale for Anxiety (HAM-A) Total Score

时间窗: Baseline (randomization) and then 8 weeks

Hamilton Rating Scale for Anxiety (HAM-A) consists of 14 items to evaluate anxiety. Each item is rated on a scale from 0-4, with '0' showing no anxiety (not present) and '4' showing the worst (very severe). Results based on MITT population with available data for this outcome measure. Least square mean of each treatment was adjusted for baseline value.

次要结局

  • Least Square Mean Change From Randomization to Week 8 in Clinical Global Impression-Severity of Illness (CGI-S) Score(Baseline (randomization) and then 8 weeks)
  • Mean Change From Randomization to Week 8 in Q-LES-Q Item 15 (Satisfaction With Medication) Score(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 1 in HAM-A Somatic Anxiety Subscale Score(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 1 in CGI-S Score(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 8 in HAM-A Psychic Anxiety Subscale Score(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 1 in HAM-A Total Score(Baseline (randomization) and then 8 weeks)
  • Number of Patients With Clinical Global Impression-Global Improvement (CGI-I) Score of "Much/Very Much Improved" at Week 8(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 8 in HAM-A Somatic Anxiety Subscale Score(Baseline (randomization) and then 8 weeks)
  • Number of Patients With HAM-A Response (≥50% Score Reduction From Randomization) at Week 8(Baseline (randomization) and then 8 weeks)
  • Number of Patients With HAM-A Remission (Total Score ≤7) at Week 8(Baseline (randomization) and then 8 weeks)
  • Mean Change From Randomization to Week 8 in Q-LES-Q Item 16 (Overall Quality of Life) Score(Baseline (randomization) and then 8 weeks)
  • Number of Patients With HAM-A Response (≥50% Score Reduction From Randomization) at Week 1(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 8 in Quality of Life Enjoyment and Satisfaction Questionaire (Q-LES-Q) Percent Maximum Total Score(Baseline (randomization) and then 8 weeks)
  • Least Square Mean Change From Randomization to Week 1 in HAM-A Psychic Anxiety Subscale Score(Baseline (randomization) and then 8 weeks)

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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