跳至主要内容
临床试验/NL-OMON26656
NL-OMON26656招募中不适用

StudY of effect of Nimodipine and Acetaminophen on Postictal Symptoms after ECT

niversity of Twente, Enschede; Rijnstate Hospital, Arnhem0 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
不适用
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

入选标准

  • Adulthood (age > 17 years);
  • Current clinical diagnosis of depressive episode (unipolar, bipolar, schizoaffective);

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

发起方
niversity of Twente, Enschede; Rijnstate Hospital, Arnhem

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