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临床试验/NCT00063362
NCT00063362终止3 期

Combination Therapy in Bipolar Rapid Cycling

University Hospitals Cleveland Medical Center0 个研究点目标入组 49 人开始时间: 2002年2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
终止
入组人数
49
主要终点
The Proportion of Patients Who Experience a Marked and Persistent Bimodal Response

研究概览

简要总结

This study will compare triple and double drug regimens in the treatment of patients with depression, hypomania, or mania.

详细描述

Early studies have shown lithium to produce a high percentage of satisfactory clinical response in patients with bipolar disorders. These studies, however, do not include lithium-refractory subgroups, such as bipolar II disorder patients. When the wide spectrum of bipolar disorders is considered, the lithium response rate decreases significantly. More broadly effective regimens are needed.

Participants in this study will be randomly assigned to receive either lithium plus divalproex or lithium, divalproex, and lamotrigine for 7 months. Symptoms of depression and mania will be assessed with scales and patient questionnaires.

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
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Bipolar I or II Disorder
  • Meet criteria for rapid cycling, defined as four or more episodes over the past 12 months
  • Meet criteria for a major depressive episode

排除标准

  • History of intolerability of lithium, divalproex, or lamotrigine

研究组 & 干预措施

Lithium + divalproex + lamotrigine

Experimental

干预措施: Lithium (Drug)

Lithium + divalproex + lamotrigine

Experimental

干预措施: Lamotrigine (Drug)

Lithium + divalproex + lamotrigine

Experimental

干预措施: Divalproex (Drug)

Lithium + divalproex + placebo

Placebo Comparator

干预措施: Lithium (Drug)

Lithium + divalproex + placebo

Placebo Comparator

干预措施: Divalproex (Drug)

Lithium + divalproex + placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

The Proportion of Patients Who Experience a Marked and Persistent Bimodal Response

时间窗: Baseline and Week 28

A marked bimodal response is defined by the following three conditions over four consecutive weeks while on triple therapy and after three weeks of ltg: 1. Montgomery Asberg Depression Rating Scale (MADRS) total score of \<= 19 2. Young Mania Rating Scale (YMRS) total score of \<= 12.5 3. Global Assessment Scale (GAS) score \>= 51 The MADRS measures the severity of a subject's depression symptoms with a possible total score ranging from 0 - 60, with higher scores indicating more severe depression. The YMRS measures the severity of a subject's manic symptoms with a possible total score ranging from 0 - 60, with higher scores indicating more severe mania. The GAS measures a used to rate subjectively the social, occupational, and psychological functioning of a subject and ranges in score from 0-100, with a higher score indicating better social, occupational, and psychological functioning.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Keming Gao

Director, Mood and Anxiety Clinic

University Hospitals Cleveland Medical Center

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