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临床试验/NCT01263080
NCT01263080已完成4 期

Multicentre Randomised Double-blind, Placebo-controlled 2x2 Factorial Trial Investigating the Effects of Adding Mirtazapine and Folic Acid to Existing Therapy for Patients With Schizophrenia

Capital Medical University1 个研究点 分布在 1 个国家目标入组 333 人开始时间: 2010年11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
333
试验地点
1
主要终点
To compare the efficacy of mirtazapine and placebo for treatment of symptoms associated with schizophrenia

研究概览

简要总结

Multicentre randomised double-blind, placebo-controlled 2x2 factorial trial investigating the effects of adding mirtazapine and folic acid to existing therapy for patients with schizophrenia

详细描述

The combination of mirtazapine plus antipsychotic potentially offers considerable benefit for patients with schizophrenia. Folic acid is a promising adjunctive therapy for schizophrenia that may also provide benefits for patients with other mental disorders. Furthermore the effects of folic acid may be affected by genotype.

The trial will investigate the effects of adding mirtazapine and the effects of adding folic acid to treatments for schizophrenia. At randomisation, patients will be separately randomised to mirtazapine or placebo and to folic acid or placebo.

Randomised, double-blind, placebo-controlled 2x2 factorial trial with 12-week follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inpatients or outpatients age 18 to 70 years;
  • Meet DSM-IV criteria for schizophrenia;
  • Signed an informed consent form by patients or their legally acceptable representatives;
  • PANSS total score >=60 and at least one item of P1, P2, P3, P5 or P6 >=4 to ensure subject has current active psychotic symptoms - i.e. hallucinations, delusions, thought disorder;
  • Subjects who are currently taking effective dose of antipsychotic;
  • Women must agree to practice an effective method of birth control if they are sexually active before entry and throughout the study.

排除标准

  • Meet any other DSM-IV Axis I disorders;
  • Meet DSM-IV criteria for substance abuse or dependence;
  • Have been treatment-resistant to 2 or more kinds of antipsychotics with sufficient dosage for at least 4 weeks, or require clozapine treatment, or have received clozapine treatment within 1 month prior to randomization;
  • Subjects are actively suicidal or judged clinically to be at risk of serious suicidal or violent behavior in the opinion of the investigator;
  • Have serious or unstable medical illness (e.g., cardiovascular disease, neurologic, hematologic, renal, hepatic, immunologic, endocrine, or other systemic illness), or have any clinically significant abnormality on laboratory test or ECG which indicate severe medical conditions;
  • Have received electroconvulsive therapy within 28 days before randomization;
  • Have received long acting antipsychotic within 1 treatment cycle before randomization;
  • Have received antidepressant within 14 days, or have received MAOIs within 4 weeks before randomization or require antidepressive treatment;
  • History of prostatic hypertrophy or dysuria;
  • History of narrow-angle glaucoma or elevation of intraocular pressure;
  • Known or suspected history of allergy or have contradiction to mirtazapine or folic acid;
  • Known have currently requirement of taking mirtazapine or folic acid;
  • Women who are pregnant or nursing;
  • Have previously completed or withdrawn from this study, or participated in a clinical trial of another drug within 30 days.

研究组 & 干预措施

mirtazapine+folic acid

Active Comparator

mirtazapine 30mg QD, folic acid 0.4mg QD

干预措施: mirtazapine (Drug)

mirtazapine+folic acid

Active Comparator

mirtazapine 30mg QD, folic acid 0.4mg QD

干预措施: folic acid (Drug)

mirtazapine+folic acid placebo

Active Comparator

mirtazapine 30mg QD, folic acid placebo 1 tablet QD

干预措施: mirtazapine (Drug)

mirtazapine+folic acid placebo

Active Comparator

mirtazapine 30mg QD, folic acid placebo 1 tablet QD

干预措施: folic acid placebo (Drug)

mirtazapine placebo+folic acid

Active Comparator

mirtazapine placebo 1 tablet QD, folic acid 0.4mg QD

干预措施: mirtazapine placebo (Drug)

mirtazapine placebo+folic acid

Active Comparator

mirtazapine placebo 1 tablet QD, folic acid 0.4mg QD

干预措施: folic acid (Drug)

mirtazapine placebo+folic acid placebo

Placebo Comparator

mirtazapine placebo 1 tablet QD, folic acid placebo 1 tablet QD

干预措施: folic acid placebo (Drug)

mirtazapine placebo+folic acid placebo

Placebo Comparator

mirtazapine placebo 1 tablet QD, folic acid placebo 1 tablet QD

干预措施: mirtazapine placebo (Drug)

结局指标

主要结局

To compare the efficacy of mirtazapine and placebo for treatment of symptoms associated with schizophrenia

时间窗: baseline, week4, week8, week12

次要结局

  • To compare the efficacy of mirtazapine and placebo for treatment of negative symptoms of schizophrenia(baseline, week4, week8, week12)
  • To compare the safety and tolerability of folic acid and placebo in patients with schizophrenia(baseline, week4, week8, week12)
  • To compare the efficacy of folic acid and placebo for treatment of symptoms of schizophrenia(baseline, week4, week8, week12)
  • To compare the efficacy of folic acid and placebo for treatment of negative symptoms of schizophrenia(baseline, week4, week8, week12)
  • To compare the safety and tolerability of mirtazapine and placebo in patients with schizophrenia(baseline, week4, week8, week12)

研究者

发起方
Capital Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gang Wang

vice-director of Affective Disorder Center, Beijing Anding Hospital

Capital Medical University

研究点 (1)

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