NL-OMON35482撤回3 期
Prevention of delirium in acute stroke - PODIAS
Kennemer Gasthuis0 个研究点目标入组 300 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 撤回
- 发起方
- 入组人数
- 300
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
- •- Patients with (suspected) stroke
- •- no delirium on admission (DRS<12; CAM < 2+1)
- •- expected duration of hospitalisation >48 hours
- •- Score on deliersticker * 5
- •- Time between admission and estimation of risk score and DRS/CAM < 24 hours
排除标准
- •- Score deliersticker < 5
- •- delirium on admission (DRS> 12; CAM * 2+1; CAM-ICU * 2 + 1)
- •- not able to perform delirum screening (DRS, CAM, CAM-ICU) on admission
- •- expected duriong of hospitalisation < 48 uur
- •- contraindication for use of haloperidol: history of allergy for haloperidol, severe liverinsufficiency, Parkinson's disease, Lewy body dementia, parkinsonism, epilepsy, use of levodopa/dopamine agonist, use of antipsychotics (e.g., haloperidol) or cholinesterase inhibitors
- •- Pronged Qt interval: Qt interval on EKG on admission * 500ms .
- •- Time between admission and estimation of risk score and DRS/CAM < 24 hours
- •- Participation in same study in the last three months
- •- severe impairment of consciousness (coma)
- •- not possible to obtain informed consent
- •- Patients, family of physician refuse to participate
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