跳至主要内容
临床试验/EUCTR2008-008366-13-DK
EUCTR2008-008366-13-DK进行中(未招募)1 期

Comparison of the effects of Sertindole and Olanzapine on Cognition - SEROLA

nit for Psychiatric Research0 个研究点目标入组 100 人开始时间: 2009年1月13日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
100

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.Both genders
  • 2.Between 18 and 65 years of age
  • 3.The ICD-10 schizophrenia diagnosis F20.0-F20.3 and F20.9 (paranoid, hebephrenic, catatonic, undifferentiated and unspecified)
  • 4.That all fertile women must use a safe form of birth control (birth control pills, spiral, gestagen depot injection, sub dermal implantation, hormonal vaginal ring and transdermal depot patch)
  • 5.A negative pregnancy test for women
  • 6.No known allergy to any of the substances in the study medication
  • 7.Baseline QTc < 450 milliseconds for men and < 470 milliseconds for women
  • 8.S-potassium and s-magnesium within normal reference range.
  • 9.Sub optimally treated on current antipsychotic medication
  • 10.Stable dosage of antidepressants and mood stabilizers one month before the inclusion
  • 11.Signed informed consent and power of attorney
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1.Withdrawal of consent
  • 2.QTc prolongation >500 milliseconds
  • 3.Patients with known clinical important cardiovascular disease e.g., heart insufficiency, cardiac hypertrophy, arrhythmia or bradycardia (<50 beats per minute)
  • 4.Significant addictions interfering with outcome and compliance
  • 5.Earlier partial or non-response in treatment or intolerability to sertindole or olanzapine.
  • 6.Calgary Depression Scale score = 7
  • 7.Treatment that interferes with the metabolism of sertindole or olanzapine, e.g. potent inhibitors of CYP1A2, CYP3A4 and CYP2D6, e.g. ketoconazole, fluvoxamine and fluoxetine as described in the SPC of Serdolect
  • 8.Oxazepam, zopiclone or zolpidem treatment the last 48 hours before cognitive testing
  • 9.Prescription of not-allowed medication, or a change in dosage of antidepressant, or mood stabilizers in the study period
  • 10.Treatment with an anticholinergic after the first three weeks of the study
  • 11.Somatic illness, as judged by investigator, interfering with cognition, e.g. delirium
  • 12.Treatment with electroconvulsive therapy (ECT) the last three months before inclusion, or treatment with ECT in the study period
  • 13.Treatment with clozapine or depot antipsychotics before inclusion

研究者

发起方
nit for Psychiatric Research

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