跳至主要内容
临床试验/NCT00926965
NCT00926965
已完成
4 期

Tardive Dyskinesia and Cognitive Function

Taipei Veterans General Hospital, Taiwan1 个研究点 分布在 1 个国家目标入组 80 人2003年1月

概览

阶段
4 期
干预措施
Olanzapine
疾病 / 适应症
Tardive Dyskinesia
发起方
Taipei Veterans General Hospital, Taiwan
入组人数
80
试验地点
1
主要终点
change of Abnormal Involuntary movement scale(AIMS), Wisconsin Card Sorting Test (WSCT) and Continuous Performance test (CPT)
状态
已完成
最后更新
16年前

概览

简要总结

Previous researchers indicate that impaired cognitive flexibility was the primary factor distinguishing patients with from those without tardive dyskinesia (TD)1, and cognitive dysfunction correlates positively with the severity of TD2. Longitudinal data raised the possibility that the association between cognitive dysfunction and TD may reflect not organic vulnerability to but rather a state marker for this movement disorder as "tardive dementia"3. Atypical antipsychotic had been reported to alleviate the severity of TD4 and improved neurocognitive function separately5. But no researchers ever investigated the correlation of the two effects simultaneously. This randomized, single-blind and controlled study compared the effect of atypical antipsychotic on TD, neurocognitive function and associated factors for these changes.

详细描述

Eighty chronic schizophrenia inpatients who received conventional antipsychotics for more than one year, and met Schooler and Kane's criteria for persistent TD were enrolled in the study. The subjects were randomized to three groups: the olanzapine, amisulpride and FGA (first generation antipsychotic) controlled groups. Neurocognitive function were assessed using Wisconsin Card Sorting Test (WSCT) and Continuous Performance test (CPT) at baseline, 12th week and 24th week. Clinical successive ratings were performed with Brief psychiatric Rating Scale (BPRS), AIMS (Abnormal Involuntary Movement Rating Scale), Simpson-Angus Rating Scale (SAS), Udvalg for Kliniske Undersogelser side effect ratings (UKU) and Barnes akathesia scale (BAS).To evaluate the influences of prognostic factors on tardive dyskinesia and neurocognitive function and to control for all potential confounding variables, longitudinal analyses on the repeated measures data were conducted using generalized estimating equation models (GEE).

注册库
clinicaltrials.gov
开始日期
2003年1月
结束日期
2007年12月
最后更新
16年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

入排标准

入选标准

  • schizophrenia inpatients who received conventional antipsychotics for more than one year,
  • those who met Schooler and Kane's criteria for persistent TD.

排除标准

  • mental retardation,
  • organic mental disorder,
  • pregnancy and allergy to trial drugs.

研究组 & 干预措施

Olanzapine group

randomized to Olanzapine group with dose range of 2.5-30mg/day

干预措施: Olanzapine

Amisulpiride group

the subjects were randomized to the amisulpiride group with dose range of 100 to 800mg/day

干预措施: amisulpride

FGA group

The subjects were randomized to maintain the conventional antipsychotics

干预措施: Conventional antipsychotics

结局指标

主要结局

change of Abnormal Involuntary movement scale(AIMS), Wisconsin Card Sorting Test (WSCT) and Continuous Performance test (CPT)

时间窗: 24 months

次要结局

  • Brief psychiatric Rating Scale (BPRS), Simpson-Angus Rating Scale (SAS), Udvalg for Kliniske Undersogelser side effect ratings (UKU) and Barnes akathesia scale (BAS).body weight, porlactin, metabolic components(24 months)

研究点 (1)

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