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临床试验/NCT00906126
NCT00906126已完成1 期

Oral Misoprostol for Labor Augmentation: A Dose-Finding Pilot Study

University of Texas Southwestern Medical Center1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2007年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
46
试验地点
1
主要终点
uterine hyperstimulation

研究概览

简要总结

A phase I, open-label trial to determine a safe dose of oral misoprostol required to augment labor in nulliparous women diagnosed with arrest of dilation.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • nulliparous
  • gestational age of at least 36 weeks
  • singleton gestation
  • cephalic presentation
  • reassuring fetal heart rate
  • 4 cm or greater cervical dilation
  • ruptured membranes with clear amnionic fluid
  • intrauterine pressure catheter in place
  • less than 200 MVU's

排除标准

  • non-reassuring fetal heart rate
  • meconium-stained amnionic fluid
  • previous uterine incision
  • maternal fever
  • pregnancy-induced hypertension or other pregnancy-related complications
  • known fetal anomalies
  • placenta previa or unexplained vaginal bleeding
  • estimated fetal weight of 4,500 grams or greater
  • evidence of cephalopelvic disproportion
  • any moderate or severe preexisting disease
  • contraindication to the use of prostaglandins

研究组 & 干预措施

Oral Misoprostol 1

Experimental

Oral misoprostol 25 micrograms every 4 hours for up to two doses.

干预措施: Misoprostol (Drug)

Oral Misoprostol 2

Experimental

Oral misoprostol 50 micrograms every 4 hours for up to two doses.

干预措施: Misoprostol (Drug)

Oral Misoprostol 3

Experimental

Oral misoprostol 100 micrograms every 4 hours for up to two doses.

干预措施: Misoprostol (Drug)

Oral Misoprostol 4

Experimental

Oral Misoprostol 50 micrograms every 2 hours for up to two doses.

干预措施: Misoprostol (Drug)

Oral Misoprostol 5

Experimental

Oral Misoprostol 75 micrograms every 4 hours for up to two doses.

干预措施: Misoprostol (Drug)

结局指标

主要结局

uterine hyperstimulation

次要结局

  • need for oxytocin augmentation
  • adequate uterine activity
  • time from administration of study drug to delivery
  • route of delivery and indications
  • maternal and neonatal infectious morbidity
  • neonatal outcomes

研究者

研究点 (1)

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