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Aripiprazole in Children and Adolescents With Bipolar I Disorder

A Phase III Trial to Test the Safety and Efficacy of Two Doses of Aripiprazole in Child and Adolescent Patients With Bipolar I Disorder, Manic or Mixed Episode With or Without Psychotic Features

The purpose of this trial is to test the safety and efficacy of two doses of aripiprazole in child and adolescent patients with bipolar I disorder, manic or mixed episode with or without psychotic features.

研究概览

研究类型

介入性

注册 (实际的)

296

阶段

  • 第三阶段

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

    • Arizona
      • Scottsdale、Arizona、美国
        • Local Institution
    • Arkansas
      • Little Rock、Arkansas、美国
        • Local Institution
    • California
      • National City、California、美国
        • Local Institution
      • Orange、California、美国
        • Local Institution
      • Pasadena、California、美国
        • Local Institution
      • Sacramento、California、美国
        • Local Institution
      • San Diego、California、美国
        • Local Institution
      • Stanford、California、美国
        • Local Institution
    • District of Columbia
      • Washington、District of Columbia、美国
        • Local Institution
    • Florida
      • Altamonte Springs、Florida、美国
        • Local Institution
      • Hialeah、Florida、美国
        • Local Institution
      • Jacksonville、Florida、美国
        • Local Institution
      • Miami、Florida、美国
        • Local Institution
      • North Miami、Florida、美国
        • Local Institution
      • Tampa、Florida、美国
        • Local Institution
    • Georgia
      • Atlanta、Georgia、美国
        • Local Institution
      • Smyrna、Georgia、美国
        • Local Institution
    • Idaho
      • Boise、Idaho、美国
        • Local Institution
    • Illinois
      • Chicago、Illinois、美国
        • Local Institution
      • Libertyville、Illinois、美国
        • Local Institution
    • Indiana
      • Indianapolis、Indiana、美国
        • Local Institution
    • Kansas
      • Kansas City、Kansas、美国
        • Local Institution
      • Newton、Kansas、美国
        • Local Institution
    • Kentucky
      • Lexington、Kentucky、美国
        • Local Institution
    • Louisiana
      • Baton Rouge、Louisiana、美国
        • Local Institution
      • Lake Charles、Louisiana、美国
        • Local Institution
      • Shreveport、Louisiana、美国
        • Local Institution
    • Massachusetts
      • Cambridge、Massachusetts、美国
        • Local Institution
      • Medford、Massachusetts、美国
        • Local Institution
    • Michigan
      • Clinton Township、Michigan、美国
        • Local Institution
      • Rochester Hills、Michigan、美国
        • Local Institution
    • Missouri
      • Kansas City、Missouri、美国
        • Local Institution
      • St. Louis、Missouri、美国
        • Local Institution
    • Nevada
      • Las Vegas、Nevada、美国
        • Local Institution
    • New York
      • Elmsford、New York、美国
        • Local Institution
      • New York City、New York、美国
        • Local Institution
      • Rochester、New York、美国
        • Local Institution
      • Stony Brook、New York、美国
        • Local Institution
    • Ohio
      • Cincinnati、Ohio、美国
        • Local Institution
      • Cleveland、Ohio、美国
        • Local Institution
    • Oklahoma
      • Oklahoma City、Oklahoma、美国
        • Local Institution
    • Pennsylvania
      • Philadelphia、Pennsylvania、美国
        • Local Institution
    • South Carolina
      • Charleston、South Carolina、美国
        • Local Institution
    • Tennessee
      • Memphis、Tennessee、美国
        • Local Institution
    • Texas
      • Bellaire、Texas、美国
        • Local Institution
      • Fort Worth、Texas、美国
        • Local Institution
      • Houston、Texas、美国
        • Local Institution
      • San Antonio、Texas、美国
        • Local Institution
    • Virginia
      • Herndon、Virginia、美国
        • Local Institution
      • Richmond、Virginia、美国
        • Local Institution
    • Washington
      • Kirkland、Washington、美国
        • Local Institution
      • Spokane、Washington、美国
        • Local Institution
    • Wisconsin
      • Milwaukee、Wisconsin、美国
        • Local Institution

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

10年 至 17年 (孩子)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Child and adolescent patients with bipolar I disorder, manic or mixed episode with or without psychotic features

Exclusion Criteria:

  • Patients with certain other psychological disorders
  • Patients with a co-morbid serious, uncontrolled systemic illness
  • Patients with significant risk of committing suicide

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:四人间

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:3个
安慰剂
Placebo tablet
有源比较器:1
Aripiprazole 10 mg tablet
Treatment Arm 1 (10 mg treatment arm): Aripiprazole 2 mg QD for 2 days, aripiprazole 5 mg QD for 2 days, and aripiprazole 10 mg QD as the target dose starting on Day 5. Subjects remained on the 10 mg dose for the remainder of the treatment period Subjects reached their target dose through a forced titration schedule and proceeded with treatment at their target dose until Week 4. If the subject reached Week 4, he or she continued into the Extension Phase, a 6-month double-blind treatment period, beginning at the same dose taken at the end of the Acute Phase.
Treatment Arm 2 (30 mg treatment arm): Aripiprazole 2 mg QD for 2 days, aripiprazole 5 mg QD for 2 days, aripiprazole 10 mg QD for 2 days, aripiprazole 15 mg QD for 2 days, aripiprazole 20 mg QD for 2 days, aripiprazole 25 mg QD for 2 days, and aripiprazole 30 mg QD as the target dose starting on Day 13. Subjects remained on the 30 mg dose for the remainder of the treatment period. Subjects reached their target dose through a forced titration schedule and proceeded with treatment at their target dose until Week 4. If the subject reached Week 4, he or she continued into the Extension Phase, a 6-month double-blind treatment period, beginning at the same dose taken at the end of the Acute Phase.
有源比较器:2
Aripiprazole 30 mg tablet
Treatment Arm 1 (10 mg treatment arm): Aripiprazole 2 mg QD for 2 days, aripiprazole 5 mg QD for 2 days, and aripiprazole 10 mg QD as the target dose starting on Day 5. Subjects remained on the 10 mg dose for the remainder of the treatment period Subjects reached their target dose through a forced titration schedule and proceeded with treatment at their target dose until Week 4. If the subject reached Week 4, he or she continued into the Extension Phase, a 6-month double-blind treatment period, beginning at the same dose taken at the end of the Acute Phase.
Treatment Arm 2 (30 mg treatment arm): Aripiprazole 2 mg QD for 2 days, aripiprazole 5 mg QD for 2 days, aripiprazole 10 mg QD for 2 days, aripiprazole 15 mg QD for 2 days, aripiprazole 20 mg QD for 2 days, aripiprazole 25 mg QD for 2 days, and aripiprazole 30 mg QD as the target dose starting on Day 13. Subjects remained on the 30 mg dose for the remainder of the treatment period. Subjects reached their target dose through a forced titration schedule and proceeded with treatment at their target dose until Week 4. If the subject reached Week 4, he or she continued into the Extension Phase, a 6-month double-blind treatment period, beginning at the same dose taken at the end of the Acute Phase.

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
Change in Young Mania Rating Scale (Y-MRS) Total Score at Week 4
大体时间:Baseline and Week 4

Change from Baseline to Week 4 in Y-MRS total score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through the continuation phase.)

The Y-MRS consists of 11 items assessing the core symptoms of mania. Each item has 5 grades of severity. Minimum score on the scale is 0 (absent or normal). Maximum score on the scale is 60 (worse outcome or more severe symptoms).

Baseline and Week 4

次要结果测量

结果测量
措施说明
大体时间
Change in Young Mania Rating Scale (Y-MRS) Total Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in Y-MRS total score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The Y-MRS consists of 11 items assessing the core symptoms of mania. Each item has 5 grades of severity. Minimum score on the scale is 0 (absent or normal). Maximum score on the scale is 60 (worse outcome or more severe symptoms).

Baseline and Week 30
Change in Children's Global Assessment Scale (CGAS) Total Score at Week 4
大体时间:Baseline and Week 4

Change from baseline to Week 4 in CGAS total score, using the last observation carried forward. Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGAS is a 100-point scale measuring psychological, social, and school functioning for children aged 6 to 17 years. Minimum scores ranged from 1-10, representing the need for constant supervision (worse outcome) to maximum scores of 91-100, representing superior functioning (better outcome).

Baseline and Week 4
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Mania Score at Week 4
大体时间:Baseline and Week 4

Change from baseline to Week 4 in CGI-BP mania score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 4
Change in Children's Depression Rating Scale-Revised (CDRS-R) Total Score at Week 4
大体时间:Baseline and Week 4
Change from baseline to Week 4 in CDRS-R score, using last observation carried forward. Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.) The CDRS-R is used to diagnose depression and monitor treatment response. The interviewer rates 17 symptom areas (including those that sever as DSM-IV criteria for diagnosis of depression), among them suicidal ideation. Minimum score on the scale is 17 (better outcome). Maximum score on the scale is 113 (worse outcome or more severe symptoms).
Baseline and Week 4
Change in General Behavior Inventory Scale (GBI) Total Parent/Guardian Version Mania Score at Week 4
大体时间:Baseline and Week 4
Change from baseline to Week 4 in GBI Total Parent/Guardian Version Mania score, using LOCF. Assessments performed baseline and weekly through acute phase (Week 4). (Also at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.) GBI is self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale was completed by parent/guardian. Symptoms rated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 4
Change in Attention Deficit Hyperactivity Disorders Rating Scale (ADHD-RS-IV) Total Score at Week 4
大体时间:Baseline and Week 4
Change from baseline to Week 4 in ADHD-RS-IV Total score, using last observation carried forward. Assessments performed at baseline and weekly through acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.) ADHD-RS-IV is an instrument for diagnosing ADHD in children/adolescents and for assessing treatment response. The scale contains 18 items linked directly to DSM-IV diagnostic criteria for ADHD. Parent questionnaire on home behaviors (Eng.) used in this study. Minimum score of 0 is a better outcome, maximum score of 54 is a worse outcome.
Baseline and Week 4
Change in Children's Global Assessment (CGAS) Total Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in CGAS total score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGAS is a 100-point scale measuring psychological, social, and school functioning for children aged 6 to 17 years. Minimum scores ranged from 1-10, representing the need for constant supervision (worse outcome) to maximum scores of 91-100, representing superior functioning (better outcome).

Baseline and Week 30
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Mania Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in CGI-BP mania score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 30
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Depression Score at Week 4
大体时间:Baseline and Week 4

Change from baseline to Week 4 in CGI-BP severity depression score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4. (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 4
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Depression Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in CGI-BP severity depression score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 30
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Overall Illness Score at Week 4
大体时间:Baseline and Week 4

Change from baseline to Week 4 in CGI-BP severity overall illness score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 4
Change in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Overall Illness Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in CGI-BP severity overall illness score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the subject's severity of illness for mania, depression, and overall bipolar illness from 1 (least severe) to 7 (most severe).

Baseline and Week 30
Change in Children's Depression Rating Scale-Revised (CDRS-R) Total Score at Week 30
大体时间:Baseline and Week 30
Change from baseline to Week 30 in CDRS-R score, using the last observation carried forward. Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. The CDRS-R is used to diagnose depression and monitor treatment response. The interviewer rates 17 symptom areas (including those that sever as DSM-IV criteria for diagnosis of depression), among them suicidal ideation. Minimum score on the scale is 17 (better outcome). Maximum score on the scale is 113 (worse outcome or more severe symptoms).
Baseline and Week 30
Change in General Behavior Inventory Scale (GBI) Total Parent/Guardian Version Mania Score at Week 30
大体时间:Baseline and Week 30
Change from baseline to Week 30 in GBI Total Parent/Guardian Version Mania score, using LOCF. Assessments performed at baseline and weekly through acute phase(Week 4) and Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale was completed by parent/guardian. Symptoms rated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 30
Change in General Behavior Inventory Scale (GBI) Total Subject Version Mania Score at Week 4
大体时间:Baseline and Week 4
Change from baseline to Week 4 in GBI Total Subject Version Mania score, using the LOCF. Assessments performed at baseline and weekly through acute phase (Week 4). (Also performed Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.) GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale completed by the subject. Symptoms rated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 4
Change in General Behavior Inventory Scale (GBI) Total Subject Version Mania Score at Week 30
大体时间:Baseline and Week 30
Change from baseline to Week 30 in GBI Total Subject Version Mania score, using LOCF. Assessments performed at baseline and weekly through acute phase (Week 4) and Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale completed by the subject. Symptoms rated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score of 0=better outcome, maximum score of 60=worse outcome.
Baseline and Week 30
Change in General Behavior Inventory Scale (GBI) Total Parent/Guardian Version Depression Score at Week 4
大体时间:Baseline and Week 4
Change from baseline to Week 4 in GBI Total Parent/Guardian Version Depression score, using LOCF. Assessments performed at baseline and weekly through the acute phase (Week 4); also Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale was completed by parent/guardian. Symptoms rated on 4-point Likert scale from 0 (never/hardly ever) to 3 (often/almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 4
Change in General Behavior Inventory Scale (GBI) Total Parent/Guardian Version Depression Score at Week 30
大体时间:Baseline and Week 30
Change from Baseline to Week 30 in GBI Total Parent/Guardian Version Depression score, using LOCF. Assessments performed at baseline and weekly through the acute phase (Week 4); also Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale completed by parent/guardian. Symptoms rated on 4-point Likert scale from 0 (never/hardly ever) to 3 (often/almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 30
Change in General Behavior Inventory Scale (GBI) Total Subject Version Depression Score at Week 4
大体时间:Baseline and Week 4
Change from Baseline to Week 4 in GBI Total Subject Version Depression score, using LOCF. Assessments performed at baseline and weekly through the acute phase (Week 4); also at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale was completed by subject. Symptoms wrated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 4
Change in General Behavior Inventory Scale (GBI) Total Subject Version Depression Score at Week 30
大体时间:Baseline and Week 30
Change from baseline to Week 30 in GBI Total Subject Version Depression score, using LOCF. Assessments performed at baseline and weekly through the acute phase (Week 4); also at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase. GBI is a self-report inventory with 73 items focused on mood-related behaviors including depressive, hypomanic, and biphasic symptoms. One 20-item subscale completed by the subject. Symptoms rated on a 4-point Likert scale from 0 (never or hardly ever) to 3 (often or almost constantly). Minimum score 0=better outcome, maximum score 60=worse outcome.
Baseline and Week 30
Change in Attention Deficit Hyperactivity Disorders Rating Scale (ADHD-RS-IV) Total Score at Week 30
大体时间:Baseline and Week 30

Change from baseline to Week 30 in ADHD-RS-IV Total score, using the LOCF.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The ADHD-RS-IV is an instrument both for diagnosing ADHD in children and adolescents and for assessing treatment response. The scale contains 18 items and is linked directly to DSM-IV diagnostic criteria for ADHD. The parent questionnaire on home behaviors (English) was used in this study. Minimum score of 0 = better outcome, maximum score of 54 = worse outcome.

Baseline and Week 30
Subject Response to Treatment at Week 4
大体时间:Baseline and Week 4

Percentage of Subjects with a 50% or higher reduction from baseline in Young Mania Rating Scale (Y-MRS) total score at Week 4.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The Y-MRS consists of 11 items assessing the core symptoms of mania. Each item has 5 grades of severity. Minimum score on the scale is 0 (absent or normal). Maximum score on the scale is 60 (worse outcome or more severe symptoms).

Baseline and Week 4
Subject Response to Treatment at Week 30
大体时间:Baseline and Week 30

Percentage of Subjects with a 50% or higher reduction from baseline in Y-MRS total score at Week 30.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The Y-MRS consists of 11 items assessing the core symptoms of mania. Each item has 5 grades of severity. Minimum score on the scale is 0 (absent or normal). Maximum score on the scale is 60 (worse outcome or more severe symptoms).

Baseline and Week 30
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Mania Score at Week 4
大体时间:Baseline and Week 4

Change from previous phase to Week 4 in CGI-BP mania score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 4
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Mania Score at Week 30
大体时间:Baseline and Week 30

Change from previous phase to Week 30 in CGI-BP mania score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 30
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Depression Score at Week 4
大体时间:Baseline and Week 4

Change from previous phase to Week 4 in CGI-BP severity depression score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 4
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Depression Score at Week 30
大体时间:Baseline and Week 30

Change from previous phase to Week 30 in CGI-BP severity depression score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 30
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Overall Illness Score at Week 4
大体时间:Baseline and Week 4

Change from previous phase to Week 4 in CGI-BP severity overall illness score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4). (Also performed at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.)

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 4
Change From Previous Phase in Clinical Global Impressions Scale-Bipolar Version (CGI-BP) Severity Overall Illness Score at Week 30
大体时间:Baseline and Week 30

Change from previous phase to Week 30 in CGI-BP severity overall illness score, using the last observation carried forward.

Assessments performed at baseline and weekly through the acute phase (Week 4) and at Weeks 6, 8, 10, 12, 16, 20, 24, and 30 through continuation phase.

The CGI-BP scale refers to the global impression of the subject with respect to bipolar disorder. The scale rates the change from the preceding phase score for mania, depression, and overall bipolar illness from 1 (very much improved) to 7 (very much worse).

Baseline and Week 30

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。

调查人员

  • 研究主任:Margaretta Nyilas, MD、Otsuka Pharmaceutical Development & Commercialization, Inc.

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

2005年3月1日

初级完成 (实际的)

2007年2月1日

研究完成 (实际的)

2007年2月1日

研究注册日期

首次提交

2005年5月9日

首先提交符合 QC 标准的

2005年5月9日

首次发布 (估计)

2005年5月10日

研究记录更新

最后更新发布 (估计)

2012年5月21日

上次提交的符合 QC 标准的更新

2012年4月19日

最后验证

2012年4月1日

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躁郁症的临床试验

  • Hospital Universitari Vall d'Hebron Research Institute
    Instituto de Salud Carlos III
    完全的
    小肠运动障碍 (Disorder)
    西班牙
  • Dren Bio
    Novotech
    招聘中
    侵袭性 NK 细胞白血病 | 肝脾T细胞淋巴瘤 | 肠病相关的T细胞淋巴瘤 | 皮下脂膜炎样 T 细胞淋巴瘤 | 单形性趋上皮性肠 T 细胞淋巴瘤 | LGLL - 大颗粒淋巴细胞白血病 | 原发性皮肤 T 细胞淋巴瘤 - 类别 | 原发性皮肤 CD8 阳性侵袭性嗜表皮 T 细胞淋巴瘤 | 系统性 EBV1 T 细胞淋巴瘤,如果 CD8 阳性 | Hydroa Vacciniforme-Like Lymphoproliferative Disorder | 结外 NK/T 细胞淋巴瘤,鼻型 | 胃肠道惰性慢性淋巴增生性疾病 (CLPD)(CD8+ 或 NK 衍生) | 上面未列出的其他 CD8+/NK 细胞驱动的淋巴瘤
    美国, 澳大利亚, 法国, 西班牙
  • Memorial Sloan Kettering Cancer Center
    招聘中
    蕈样肉芽肿 | 塞扎里综合症 | 血管免疫母细胞性T细胞淋巴瘤 | 肝脾T细胞淋巴瘤 | 间变性大细胞淋巴瘤,ALK 阳性 | 结外 NK/T 细胞淋巴瘤,鼻型 | T细胞淋巴瘤 | 未特指的外周 T 细胞淋巴瘤 | 原发性皮肤间变性大细胞淋巴瘤 | 皮下脂膜炎样 T 细胞淋巴瘤 | 肠病相关的T细胞淋巴瘤 | 间变性大细胞淋巴瘤,ALK 阴性 | 单形性趋上皮性肠 T 细胞淋巴瘤 | T 细胞幼淋巴细胞白血病 | T 细胞大颗粒淋巴细胞白血病 | 原发性皮肤 CD8 阳性侵袭性嗜表皮 T 细胞淋巴瘤 | Hydroa Vacciniforme-Like Lymphoproliferative Disorder | NK细胞淋巴瘤 | 侵袭性 NK 细胞白血病 | 成人 T 细胞白血病/淋巴瘤 及其他条件
    美国
3
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