NL-OMON48237招募中2 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: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 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
入排标准
- 年龄范围
- 18 至 99（—）
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.
排除标准
- •Known adverse reactions to acetaminophen or nimodipine. In that case
- •participants can still be included into the other intervention groups;
- •Chronic use of acetaminophen, calcium-antagonists or NSAID*s that cannot be
- •interrupted for less than two days before the ECT-session.
研究者
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