NL-OMON44544已完成不适用
Effect of perioperative ketamine on postoperative cognition * a randomized placebo-controlled trial - Proket study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
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 planned for elective surgery lasting > 1 h that require postoperative pain relief will be enrolled in the study after written informed consent is obtained.
排除标准
- •* age < 54 years,
- •* body mass index > 35 kg/m2,
- •* history or present psychiatric disease,
- •* untreated/uncontrolled hypertension (with a diastolic blood pressure > 100 mmHg), epilepsy,
- •* increased intracranial pressure,
- •* untreated hypertension,
- •* untreated ischemic cardiac disease,
- •* inability to communicate in the Dutch language,
- •* inability to give informed consent.
- •* Known liver disease
- •* inability to wear the RespiR8 mask
研究者
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