跳至主要内容
临床试验/EUCTR2014-003008-53-NL
EUCTR2014-003008-53-NL进行中(未招募)不适用

Clonidine Augmentation Therapy in Schizophrenia - CATS (Clonidine Augmentation Therapy in Schizophrenia)

niversity Medical Center Utrecht0 个研究点目标入组 75 人开始时间: 2014年9月10日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
75

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. A DSM-IV-R diagnosis of: 295.x (schizophrenia, schizophreniform disorder, or
  • schizoaffective disorder)
  • 2. No or only partial response to clozapine as defined by a total PANSS score of at least 80.
  • 3. Age 18-45 years.
  • 4. Patients are treated with antipsychotic medication
  • 5. Written informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 75
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Presence of any of the contra-indications of clonidine as reported in the Summary of Product Characteristics (SPC).
  • 2. Supine systolic blood pressure (SSBP) < 85 mm HG
  • 3. Pre-existent orthostatic hypotension with a drop of systolic blood pressure of > 20 mmHg or a drop of diastolic blood pressure of >10 mmHg.
  • 4. Supine heart rate (SHR) < 50 beats/min
  • 5. Severe brady-arhytmias such as sick-sinussyndroom, second or third degree AV-block.
  • 6. Pregnancy or breast-feeding. A urine pregnancy test will be performed at screening.

研究者

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