跳至主要内容
临床试验/PACTR202308755450519
PACTR202308755450519尚未招募Unknown

Comparing the efficacy of Intravenous Paracetamol to Imtramuscular Pethidine for labour analgesia in ILorin: A randomized controlled study.

Self funded0 个研究点目标入组 96 人开始时间: 2023年7月24日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
96

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

  • INCLUSION CRITERIA
  • Women with term gestation (37 to 42 weeks), with singleton fetus in cephalic presentation
  • Women who present in active phase of labour (cervical dilatation of 4-6cm), either spontaneous or induced
  • Consent to participate in the study.

排除标准

  • EXCLUSION CRITERIA
  • Women with cervical dilatation of 7cm or more.
  • Multiple gestation.
  • Women with previous uterine surgery (caesarean section, myomectomy).
  • Women with antepartum haemorrhage in index pregnancy.
  • History of hyper-sensitivity to PCM and/or pethidine.
  • Women with diagnosed liver disease and / or sickle cell disease patient.

研究者

发起方
Self funded

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