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临床试验/NCT01063244
NCT01063244已完成3 期

Comparison of Foley Balloon With or Without Traction for the Cervical Ripening

St. Luke's Hospital, Pennsylvania2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2009年1月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
65
试验地点
2
主要终点
Time to effectively ripen cervix

研究概览

简要总结

We will compare the use of foley bulb catheters placed in the cervix for ripening of the cervix for labor induction,.

详细描述

One arm will have the foley balloon placed alone in the cervix. And one arm will have the foley balloon placed in the cervix and then attached to a weight (1000 cc Iv Bag of fluid). Our hypothesis is that the weighted balloon will be more effective than the non-weighted balloon in the ripening of the cervix for induction of labor

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Term pregnancy scheduled for induction of labor

排除标准

  • Preterm pregnancy that require induction for fetal indications

结局指标

主要结局

Time to effectively ripen cervix

时间窗: to effective cervical ripening

次要结局

未报告次要终点

研究者

发起方
St. Luke's Hospital, Pennsylvania
申办方类型
Other
责任方
Principal Investigator
主要研究者

James Anasti, MD

Director, OB?GYN Residency Program

St. Luke's Hospital, Pennsylvania

研究点 (2)

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