EUCTR2009-014532-37-DE进行中(未招募)不适用
Effekte von oraler Cortisol oder Propranolol-Gabe auf die Verarbeitung alkoholbezogener Schlüsselreize, den Schlaf und das Rückfallrisiko von alkoholabhängigen Patienten (Copro-Studie). - Copro-Studie
niversitätsklinikum Schleswig-Holstein0 个研究点开始时间: 2010年10月5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)
- 发起方
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
- Male
入选标准
- •alcohol dependence,
- •abstention for 3 das minimum before entering the study,
- •male subject,
- •age in the rage 18 to 55 years
- •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
- •relevant psychiatric or organic comorbidities that might influence outcome and that might be negatively influenced by study medication e.g. depression, schizophrenia, obsessive comlusive disorder, anorexia, anxiety disorder, dementia, liver-cirrhosis, heart failure, epilepsy, dependence from other legal or illicit drugs.
研究者
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