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临床试验/NCT00338949
NCT00338949已完成4 期

The Metabolic Syndrome in Patients With Schizophrenia

Veterans Medical Research Foundation1 个研究点 分布在 1 个国家目标入组 77 人开始时间: 2006年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
77
试验地点
1
主要终点
Change in Insulin Sensitivity Index From Baseline to Week 26 ((1/mU/L) x 1/Min)

研究概览

简要总结

This study will evaluate the effectiveness of ziprasidone treatment versus treatment with a standard atypical antipsychotic drug in improving insulin sensitivity and reducing excess abdominal fat storage in people with schizophrenia who are at risk for diabetes.

详细描述

People with schizophrenia often lead more sedentary lifestyles than people without the disease, and they are frequently treated with antipsychotic medications that cause weight gain. Combined, these factors produce an increased risk for metabolic syndrome, which can lead to heart disease and type 2 diabetes. Characteristics of metabolic syndrome include carrying excess weight around the abdominal region; high blood pressure; high blood sugar levels; high levels of fat in the blood; and low levels of HDL cholesterol. Recent studies have shown that certain atypical antipsychotic drugs are relatively weight-neutral. Switching from a drug that promotes weight gain to a weight-neutral medication, such as ziprasidone, may result in significant weight loss. There is insufficient evidence, however, demonstrating the extent of improvement in insulin sensitivity after switching medications. This study will evaluate the effectiveness of ziprasidone treatment versus treatment with a standard atypical antipsychotic drug in improving insulin sensitivity and reducing excess abdominal fat storage in people with schizophrenia who are at risk for diabetes.

Participants in this open label study will currently be undergoing treatment with risperidone or olanzapine at the time of study entry. Upon study entry, they will be randomly assigned to either switch to ziprasidone treatment or remain on their current medications. Both groups will be treated for 26 weeks. Participants will report to the study site for evaluations biweekly until week 10 and then monthly for the duration of the study. The primary outcomes at Week 26 will be: change from baseline in insulin sensitivity, using an intravenous glucose tolerance test; change from baseline in ivisceral fat mass, using a CT scan.

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
None

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

  • Diagnosis of schizophrenia or schizoaffective disorder
  • Currently receiving antipsychotic therapy with risperidone or olanzapine
  • Overweight

排除标准

  • Diagnosis of diabetes
  • Hospitalization for schizophrenia or schizoaffective disorder within 90 days prior to study entry
  • Refractory schizophrenia or schizoaffective disorder
  • Currently receiving therapy with clozapine
  • No stable residence and phone number for 90 days prior to study entry
  • Prior unsuccessful treatment with ziprasidone
  • Intolerance to ziprasidone

研究组 & 干预措施

Control

Active Comparator

Participants on risperidone or olanzapine who will remain on risperidone or olanzapine and do not switch to ziprasidone

干预措施: Control (Drug)

Switch

Experimental

Participants who enter on risperidone or olanzapine and switch to ziprasidone

干预措施: Switch (Drug)

结局指标

主要结局

Change in Insulin Sensitivity Index From Baseline to Week 26 ((1/mU/L) x 1/Min)

时间窗: Measured at Baseline and Week 26

As measured by frequently sampled intravenous glucose tolerance testing (units: 1/mU/L) x 1/Min)

Change in Visceral Fat Mass From Baseline to Week 26

时间窗: Baseline and Week 26

CT measured change in visceral fat mass from baseline to week 26 (mm\^3)

次要结局

未报告次要终点

研究者

发起方
Veterans Medical Research Foundation
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jonathan M. Meyer, MD

Research Scientist

Veterans Medical Research Foundation

研究点 (1)

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