EUCTR2019-000617-37-NL进行中（未招募）1 期
StudY of effect of Nimodipine and Acetaminophen on Postictal Symptoms after ECT - SYNAPSE
Rijnstate ziekenhuis0 个研究点目标入组 33 人开始时间: 2019年7月25日最近更新:
适应症
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
- 33
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
入选标准
- •Adulthood (age > 17 years);
- •Current clinical diagnosis of depressive episode (unipolar, bipolar, schizoaffective);
- •Willingness and ability to give written informed consent and willingness and ability to understand, to participate and to comply with the study requirements.
- •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 17
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 16
排除标准
- •Known adverse or allergic reactions to acetaminophen or nimodipine;
- •Chronic use of acetaminophen,calcium-antagonistsor NSAID’s that cannot be interrupted for less than two daysbefore the ECT-session;
- •Contraindications for magnetic resonance imaging (e.g. ferromagnetic implants, pacemakers).
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