ACTRN12615000505505已完成未知
The Relationship between Sleep Quality and Target Effect-site Propofol Concentration of Target-Controlled Infusion in Adult Female Patients Receiving Transvaginal Oocyte Retrieval
Changhua Christian Hospital, Taiwan (R.O.C.)0 个研究点目标入组 200 人开始时间: 2015年5月20日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 20 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •Female patients assessed as the American Society of Anesthesiologists (ASA) physical status classification system class I and II who are ready for transvaginal oocyte retrieval
排除标准
- •(1) refusal to provide informed consent,
- •(2) allergy to intravenous propofol, fentanyl, or lidocaine,
- •(3) hepatic, renal, or neurological dysfunction
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