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临床试验/PACTR202306521096535
PACTR202306521096535已完成Unknown

A randomized controlled trial between epidural bupivacaine and intravenous bupivacaine for labour analgesia.

Olakunle Azeez0 个研究点目标入组 114 人开始时间: 2023年2月15日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
114

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
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • The inclusion criteria were:
  • 1). Consenting nulliparous women age between 18 and 35years.
  • 2). Women with a singleton fetus in cephalic presentation.
  • 3). Women in established spontaneous labour at term and cervical dilatation of 4-6cm.
  • 4). Women whose anaesthetic risk assessment is ASA physical status class II

排除标准

  • The exclusion criteria were:
  • 1). Women who do not consent
  • 2). Women with weights greater than 90kg
  • 3). Women with heights less than 1.5m.
  • 4). Women with complicated pregnancies that require emergency management
  • 5). Women with contraindications to epidural analgesia or opioid administration.

研究者

发起方
Olakunle Azeez

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