EUCTR2005-005400-17-DK进行中（未招募）1 期
Optimizing propofol in obese patients
Dept. of Anaesthesia, Center of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet0 个研究点目标入组 38 人开始时间: 2005年12月6日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 38
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Elective abdominal non-laparoscopic hysterectomia
- •Age>18 years
- •ASA physical status I-III
- •Body Mass Index =30
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Allergic towards propofol
- •Daily consumption of benzodiazepine (more than at nighttime), opioids or amphetamine preoperatively.
- •Disease with expected EEG-abnormality or impaired auditory function: Epilepsy, deafness, previous neurosurgery, previous or actual neurologic disease with neurologic deficit.
研究者
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