EUCTR2004-003776-10-LV进行中（未招募）不适用
Safety amd tolerability of ocaperidone in the continuation treatment of patients with schizophrenia: a double-blind, parallel group, multicentre, fixed dose, follow-up study
euro3d0 个研究点目标入组 20 人开始时间: 2005年1月24日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 20
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
- •- patients who completed study N3D/FOR-OCA-05;
- •- patients who are BPRS responders and tolerated treatment well in study N3D/FOR-OCA-05;
- •- patients must have given written informed consent prior to screening assessments;
- •- a legal representative (guardian or relative) can consent on behalf of the patient if he/she is unable to provide written 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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- any patient who was never included in study N3D/FOR-OCA-05
- •- any patient who had a premature termination in prior study N3D/FOR-OCA-05 must not be included in N3D/FOR-OCA-08 study
研究者
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