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临床试验/PACTR202203615684194
PACTR202203615684194已完成未知

Intramuscular Paracetamol Versus Intramuscular Tramadol as an Intrapartum Labour Analgesia: A Randomised Controlled Trial

Ebere Ikenna0 个研究点目标入组 140 人开始时间: 2022年3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
140

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

  • 1) booked pregnant women
  • 2) spontaneous onset of labour
  • 3) term singleton fetus, in cephalic presentation
  • 4) no contraindication to vaginal delivery
  • 5) consent to participate in the study.

排除标准

  • 1.Refusal to give consent
  • 2.Patients with multiple gestation
  • 3.Patients who presented at a gestational age below 37 weeks
  • 4.Patients with history narcotics dependency
  • 5.Patients with cardiopulmonary depression
  • 6.Fetal distress
  • 7.Intrauterine fetal death
  • 8.Antepartum haemorrhage
  • 9.History of recent chronic liver disease
  • 10.Vaginal birth after Caeserean section
  • 11.Breech presenting fetuses
  • 12.History of renal disease
  • 13.Known allergy to acetaminophen/tramadol
  • 14.Any contraindication to vaginal delivery
  • 15.Induced labour

研究者

发起方
Ebere Ikenna

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