Quetiapine Augmentation for Primary Anxiety Disorder or Mood Disorders With Co-morbid Anxiety Symptoms
2012年1月3日 更新者:Chih-Ken Chen、Chang Gung Memorial Hospital
Quetiapine Augmentation for Primary Anxiety Disorder or Mood Disorders With Comorbid Anxiety Symptoms
The objectives of this study are to evaluate the efficacy and safety of quetiapine extended release tablet versus placebo as adjunct to selective serotonin reuptake inhibitors/serotonin/norepinephrine reuptake inhibitors (SSRI/SNRI) in the augmentation treatment of patient with primary anxiety disorders or mood disorders with co-morbid anxiety symptoms.
研究概览
地位
完全的
研究类型
介入性
注册 (实际的)
39
阶段
- 第四阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
-
Keelung、台湾
- Chang Gung Memorial Hospital - Keelung
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 65年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Provision of written informed consent
- A diagnosis of primary anxiety disorder or mood disorder with co-morbid anxiety symptoms by Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition (DSM-IV)
- A 14-item Hamilton Anxiety Scale (HAM-A)>= 14
- Subject have received single antidepressant at a therapeutic dose for at least 6 weeks
- Male or female aged 18-65 years
- Female patients of childbearing potential must be using a reliable method of contraception and have a negative urine human chorionic gonadotropin (HCG) test at enrollment
- Able to understand and comply with the requirements of the study and sign informed consent
Exclusion Criteria:
- Pregnancy or lactation
- Any DSM-IV Axis I disorder not defined in the inclusion criteria.
- Receiving any anti-psychotic 7 days prior to entering the study
- Patients who, in the opinion of the investigator, post an imminent risk of suicide or a danger to self or others
- Known intolerance or lack of response to quetiapine fumarate, as judged by the investigator
- Use of any of the following cytochrome P450 3A4 inhibitors in the 14 days preceding enrollment including but not limited to: ketoconazole, itraconazole, fluconazole, erythromycin, clarithromycin, troleandomycin, indinavir, nelfinavir, ritonavir, fluvoxamine and saquinavir
- Use of any of the following cytochrome P450 3A4 inducers in the 14 days preceding enrollment including but not limited to: phenytoin, carbamazepine, barbiturates, rifampin, St.John's Wort, and glucocorticoids
- Administration of a depot antipsychotic injection within one dosing interval (for the depot) before randomization
- Substance or alcohol dependence at enrollment (except dependence in full remission, and except for caffeine or nicotine dependence), as defined by DSM-IV criteria
- Opiates, amphetamine, barbiturate, cocaine, cannabis, or hallucinogen abuse by DSM-IV criteria within 4 weeks prior to enrollment
- Medical conditions that would affect absorption, distribution, metabolism, or excretion of study treatment
- Unstable or inadequately treated medical illness (e.g. congestive heart failures, angina pectoris, hypertension) as judged by the investigator
- Involvement in the planning and conduct of the study
- Previous enrollment or randomization of treatment in the present study
- Participation in another drug trial within 4 weeks prior enrollment into this study or longer in accordance with local requirements
A patient with Diabetes Mellitus (DM) fulfilling one of the following criteria:
- Unstable DM defined as enrollment glycosylated hemoglobin(HbA1c)> 8.5%
- Admitted to hospital for treatment of DM or DM related illness in past 12 weeks.
- Not under physician care for DM
- Physician responsible for patient's DM care has not indicated that patient's DM is controlled
- Physician responsible for patient's DM care has not approved patient's participation in the study
- Has not been on the same dose of oral hypoglycaemic drug(S) and/or diet for the 4 weeks prior to randomization. For thiazolidinediones(glitazones) this period should not be less than 8 weeks
- Taking insulin whose daily dose on one occasion in the past 4 weeks has been more than 10% above or below their mean dose in the preceding 4 weeks
- An absolute neutrophil count (ANC) of <= 1.5x10(9) per liter
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Quetiapine extended release tablet
Quetiapine orally at a flexible dose fo 50-300mg/day according to the judgment by the investigator for 8 weeks, as adjunct to the same antidepressant at the same dose.
|
Quetiapine extended release tablet of 50-300mg/day
|
|
安慰剂比较:Placebo
Placebo orally, as adjunct to the same antidepressant at the same dose.
|
Placebo orally, as adjunct to the same antidepressant at the same dose.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Hamilton Anxiety Scale(HAMA-A) total score
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Item scores for Abnormal Involuntary Movement Scale(AIMS)
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
|
Item scores of Barnes-Akathisia Rating Scale (BARS)
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
|
Item scores of Simpson-Angus Scale(SAS)
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
|
Body Weight
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
|
Vital signs
大体时间:2 months
|
From baseline to Week 1, Week 4 and Week 8
|
2 months
|
|
Adverse event/Serious adverse event
大体时间:8-9 weeks
|
From the time Informed Consent has been obtained to Week 1, Week 4 and Week 8
|
8-9 weeks
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
合作者
调查人员
- 首席研究员:Chih-Ken Chen, MD, PhD、Chang Gung Memorial Hospital
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2009年5月1日
初级完成 (实际的)
2010年7月1日
研究完成 (实际的)
2010年7月1日
研究注册日期
首次提交
2009年5月24日
首先提交符合 QC 标准的
2009年5月31日
首次发布 (估计)
2009年6月3日
研究记录更新
最后更新发布 (估计)
2012年1月5日
上次提交的符合 QC 标准的更新
2012年1月3日
最后验证
2012年1月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.