TCTR20210705001已完成1 期
Efficacy of the enhanced recovery after surgery (ERAS) protocol following elective cesarean section, a single-center randomized controlled trial
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 48
研究概览
简要总结
o difference in QoR-35, Better in pain score in ERAS group and no difference in complication after sergery
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 Years 至 40 Years（—）
- 性别
- Female
入选标准
- •i)Women aged 20-40 years
- •ii)Singleton pregnancy without severe obstetric (Gestational diabetic mellitus) or severe medical complications such as kidney disease, asthma, heart disease, pregestational diabetic mellitus
排除标准
- •i)subsequently had postpartum hemorrhage,
- •ii)Received (or be converted to) general anesthesia,
- •iii)Underwent emergency cesarean section, or iv) demonstrated unstable post-operative condition (shock, anaphylaxis, respiratory distress)
- •iv)Contraindication to use cefazolin, NSAIDs, metoclopramide,
- •v)Cannot read Thai questionnaire,
- •vi)Refuse to joint research
研究者
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