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临床试验/PACTR201710002424167
PACTR201710002424167已完成未知

Maternal and fetal outcomes in three regimens for intrathecal analgesia in multipara women undergoing normal vaginal delivery

Faculty of Medicine0 个研究点目标入组 100 人开始时间: 2017年7月13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
100

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 35 Year(s)(—)
性别
Female

入选标准

  • Multipara woman, ASA physical status I or II,
  • in active labor with engaged fetal head, term pregnancy of singleton fetus not in distress (Normal cardiotocography [baseline fetal heart rate between 110 and 160 beats/minute, baseline variability >5 beats/minute, presence of accelerations, and absence of decelerations],
  • minimal cervical dilatation of at least 3 cm with intact membranes,
  • those requiring oxytocin augmentation, cephalic presentation, and uncomplicated pregnancies.

排除标准

  • Patients who refuse to participate, preexisting or pregnancy-induced hypertension,
  • endocrine diseases,
  • diagnosed fetal abnormalities,
  • contra-indications to neuraxial anesthesia, occurrence of wet tap during epidural placement,
  • fade of spinal analgesia & hence need for epidural activation,
  • previous systemic opioid administrations, allergy to study agents,
  • unconscious parturients,
  • patients who are unable to communicate.

研究者

发起方
Faculty of Medicine

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