NL-OMON54344招募中不适用
Prediction of ECT treatment response and reduction of Cognitive Side-effects using EEG and Rivastigmine - PRECISER
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 100
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 64（—）
入选标准
- •- Ageover 18 years
- •- Clinical indication for ECT (as indicated by the treating
- •physician/psychiatrist)
- •- Depressive disorder (as assessed by the treating psychiatrist)
- •- Dutch as first language
排除标准
- •- Currently using rivastigmine, galantamine, donezepil (all cholinesterase
- •inhibitors for mild to moderate Alzheimer*s Disease).
- •- Pregnancy and/or lactation/breast feeding
- •- Suspicion of neurodegenerative disorders (as diagnosed earlier)
- •- Contraindications for ECT (recent myocardinfarct, recent cerebrovasculair
- •accident, recent intracranial surgery, pheochromocytoma and instable angina
- •- Contraindications for rivastigmine (bradycardia or atrioventricular (AV)
- •conduction disorders (first degree AV-block excluded))
- •- Patients who have had an allergic reaction to rivastigmine
- •- Cognitive disorder not explained by the depressive episode
- •- If receiving outpatient ECT treatment, having no person available to
- •apply the rivastigmine/non-active patch
研究者
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