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临床试验/ISRCTN10109823
ISRCTN10109823终止未知

Pilot comparative study on patient satisfaction with Cervical Ripening Balloon using inpatient and outpatient protocol

ational Maternity Hospital0 个研究点目标入组 40 人开始时间: 2018年5月29日最近更新:

试验速览

阶段
未知
状态
终止
发起方
入组人数
40

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

性别
Female

入选标准

  • 1. Nulliparous women with singleton pregnancies
  • 2. Aged 18 to 40 years
  • 3. The fetus is in cephalic presentation
  • 4. Low risk pregnancies going for induction of labour for postdates pregnancies as per protocol in National Maternity Hospital

排除标准

  • 1. Any pre-existing medical condition or medical condition of pregnancy
  • 2. Pathological CTG prior to induction
  • 3. Oligohydramnios or any other abnormal findings on post-dates scan
  • 4. Maternal age <18 years old or >40 years old

研究者

发起方
ational Maternity Hospital

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