ISRCTN16067539已完成不适用
The analgesic efficacy of a low dose of bupivacaine plus fentanyl versus a conventional dose of bupivacaine plus fentanyl for subarachnoid anaesthesia during caesarean section: A controlled clinical trial
eiva City University Hospital (Colombia)0 个研究点目标入组 65 人开始时间: 2011年2月28日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 65
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
- 性别
- Female
入选标准
- •1. Pregnant patients over 18 years with an indication of caesarean section
- •2. ASA II patient
排除标准
- •1. Patient who refused to enter the study
- •2. Patients with known hypersensitivity to any of the anesthetic agents used in the study
- •3. Patients with contraindication to spinal block
- •4. Procedures lasting more than an hour
- •5. Patients with multiple pregnancy or premature birth
- •6. Patients receiving non-steroidal anti-inflammatory drugs (NSAIDs) and / or opioids intravenous(IV) in the last 4 hours
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