NL-OMON33167已完成不适用
A double-blind functional MR study to investigate the stability of the signal at baseline and following the administration of cognitive tests in placebo condition and after oral administration of a benzodiazepine in young healthy male subjects - Reproducibility of cognitive fMRI tests after placebo and benzodiazepine
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 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
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Healthy, right-handed male individuals between 18-25 year -o.
排除标准
- •Female sex.
- •Previous participation in a study with MRI.
- •Clinically significant history of drug allergies (benzodiazepines).
- •Recent history (within previous 6 months) of alcohol or drug abuse.
- •History of or current significant medical illness including cardiac arrhythmias or other cardiac disease, hematological disease, bronchospastic respiratory disease, dyspnea, diabetes mellitus, renal or hepatic insufficiency, thyroid disease, infection, or any other illness that the investigator considers clinically significant.
- •History of or current psychiatric or neurological illness.
- •Smoking cigarettes (or equivalent) or the use of nicotine based products, within 3 months prior to study drug administration
- •Positive urine screen for drugs of abuse at screening or admission.
- •Use of any prescription or over-the-counter psychotropic medication (including herbal medications) within 2 weeks of dosing with the study drug.
- •Visual disorder that cannot be corrected through the use of corrective lenses
- •Claustrophobia and/or a panic disorder
- •Those suffering from phobiae of physical restraint, specifically concerning the head and the hand/finger complex
- •Participants who do not fulfill the criteria for participating in an fMRI assessment (e.g. people who have metal implants (pacemaker, heartvalves, vascular clips, eye-implants or red tattoos, piercing)
- •Psychological and/or emotional problems, which limit the ability of the subject to comply with the study requirements.
- •Any condition that, in the opinion of the investigator, would compromise the well-being of the subject or the study
研究者
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