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临床试验/IRCT2015080423444N1
IRCT2015080423444N1已完成未知

The effect of intravenous Hyoscine-N-butylbromide on active phase labor pain in primigravid women

Zahedan University of Medical Sciences0 个研究点目标入组 105 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
105

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

  • Term pregnancy (37-42 weeks), pregnancy with a single live fetus, cephalic presentation, intact membrance, enter in the active phase of labor( cervical dilatation of 4 cm) with uterine contraction (at least 3 contraction lasting 40-60 seconds in 10 minutes), estimated fetal weight between 2500-4500 gr and absence of contraindication for vaginal delivery were the criteria for inclusion. The women with chronic induced illnesses, severe prepartum hemorrhage, preeclampsia, emergency cesarean section, prior uterine scar and the need to use other methods of analgesia (epidural analgesia or other opioids) were evicted from the study.

排除标准

  • 未提供

研究者

发起方
Zahedan University of Medical Sciences

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