跳至主要内容
临床试验/ACTRN12609000153213
ACTRN12609000153213已完成1 期

Randomized prospective, double blind, placebo-controlled study to compare the efficacy and safety of meperidine and valethamate bromide with placebo for acceleration of labor.

Dr Sefa Kelekci0 个研究点目标入组 39 人开始时间: 2009年3月18日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
39

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 30 Years(—)
性别
Female

入选标准

  • otherwise healthy nulliparous women undergoing labor induction between 18 and 30 years old with a term singleton pregnancy, vertex presentation

排除标准

  • spontaneous labor, estimated fetal weight > 4000 g, suspicion of cephalopelvic disproportion (CPD), evidence of fetal distress, meperidine or valethamate bromide allergy, previous uterine surgery, active vaginal bleeding, placenta praevia, and use of any kind of analgesia prior randomization.

研究者

发起方
Dr Sefa Kelekci

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