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临床试验/PACTR201702002020948
PACTR201702002020948已完成未知

Maternal and fetal outcome with the use of Fentanyl versus Pethidine for pain relief during labour: a randomized clinical trial

Faculty of Medicine0 个研究点目标入组 300 人开始时间: 2017年2月6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
300

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 Year(s) 至 32 Year(s)(—)
性别
Female

入选标准

  • women who were in the active labour (defined as regular uterine contractions of at least two in ten minutes), with a singleton pregnancy, cervical dilatation of at least four cm, with gestation of 37¿41 weeks, and reactive non-stress test.

排除标准

  • included allergy or previous adverse reaction to opioids or opioid dependency, use of parenteral opioids within the previous 24 hours, presence of severe systemic or mental disease, maternal respiratory rate ¿ 8 or maternal bradycardia (pulse rate less than 60), and women requesting additional dosage of analgesia. The authors excluded women requesting additional analgesia in order to test the specific single dosing for a particular opioid.

研究者

发起方
Faculty of Medicine

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