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临床试验/IRCT20220308054220N1
IRCT20220308054220N1尚未招募3 期

EFFICACY OF PARENTERAL ACETAMINOPHEN AS INTRAPARTUM ANALGESIC

Public sector medical college Rawalpindi Pakistan0 个研究点目标入组 130 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
130

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 years 至 35 years(—)
性别
Female

入选标准

  • Primigravida of 18–35 year.
  • Full-term with uncomplicated spontaneous onset of labour at term (37–42 weeks gestation).
  • Singleton pregnancy.
  • Cervical dilatation of 3-5 cm.
  • Cephalic presentation of fetus.

排除标准

  • Malpresentation of fetus.
  • Multiparous women.
  • Previously scarred uterus (post myomectomy, post cesarean).
  • Preterm labour.
  • Antepartum hemorrhage.
  • History of drug allergy or hypersensitivity.
  • Fetal distress (abnormal foetal monitoring during labour).
  • Intrauterine foetal death.
  • Refusal by parturient.
  • History of alcohol/drug abuse.
  • Systemic and local sepsis.
  • Deranged coagulation profile.
  • Obstetric complications (e.g., premature rupture of amniotic membranes).
  • Women with clinical evidence of cephalopelvic disproportion.

研究者

发起方
Public sector medical college Rawalpindi Pakistan

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