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临床试验/NCT03310333
NCT03310333Unknown4 期

Comparison Between Two Strategies of Induction in Case of Unfavourable Cervix After 12 Hours of Premature Rupture of Membranes (PROM) at Term: Cook Cervical Ripening + Oxytocine From 6 Hours Versus Dinoprostone Vaginal Insert

University Hospital, Clermont-Ferrand1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2018年2月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
80
试验地点
1
主要终点
Time between the beginning of the induction of labor and the delivery

研究概览

简要总结

The objective is to demonstrate the superiority of the strategy of labor induction by Cook® cervical ripening balloon between recommended strategy by dinoprostone (propess®) on the reduction of the time between cervical ripening and delivery in case of unfavorable cervix after 12 hours of PROM in term pregnant women.

详细描述

The inclusion begins after 12 hours of PROM for a pregnant woman who has an unfavourable cervix and no B streptococcus. The case is discussed during the obstetric staff every morning.

If the cervix is unfavourable (cervical Bishop's score <6), the information of the study is given to the patient and the consent collected.

An antibiotic is started at the beginning of the inclusion by amoxicillin (or clindamycin in case of allergy of amoxicillin) to prevent choroamnionitis.

After randomization, the patient is included in one of the two groups: Cook ® balloon or Propess ®.

  • In the Cook cervical ripening balloon group: the device is introduced by a resident or a doctor. No traction on the probe was done. It is left in place for maximum 12 hours. Oxytocin is added at the end of the first 6 hours even if device is fallen. An epidural analgesia can be started before or after the installation of oxytocin
  • In dinoprostone vaginal group: the device is placed in vaginal fornix by the midwife for maximum 24 hours. If Propess ® is fallen before the first 12 hours, another one could be introduce if the cervix stayed unfavourable.

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

盲法说明

open

入排标准

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

入选标准

  • Pregnant women
  • 18 years old With a singleton live cephalic pregnancy ≥ 37+0 weeks Gestational age estimated from the first trimester ultrasound (realized between 11 and 13+6 weeks of gestation) PROM without spontaneous labour in the 12 hours after the rupture. The diagnostic of PROM is clinic or biologic (ActimProm® test).
  • Unfavourable cervix (Bishop's score < 6) Agreement of the patient after clear, loyal and appropriate information Subject covered by or having the rights to the French Social Security system

排除标准

  • Vaginal infection by B streptococcus or in urinary sample during actual or anterior pregnancy Meconium fluid amniotic Contraindication of vaginal delivery (placenta praevia, ...) Temperature > 38,2°C Suspicion of chorio-amnionitis among Newton requirements Intra-uterine growth restriction < 3rd percentile with Doppler abnormalities History of cesarean and uterine scare Suspected genital herpes infection Known VIH seropositivity (confirmed by blood serology) Fetus with suspected severe congenital abnormalities Pathological fetal heart rate (see appendix 1) Contra-indications to Propess®, Cook® Cervical Ripening Balloon, Oxytocin Women under guardianship or trusteeship

研究组 & 干预措施

Cook cervical ripening

Experimental

the device is introduced by a resident or a doctor. No traction on the probe was done. It is left in place for maximum 12 hours. Oxytocin is added at the end of the first 6 hours even if device is fallen. An epidural analgesia can be started before or after the installation of oxytocin

干预措施: cook cervical pipening balloon (Device)

Dinoprostone vaginal group

Active Comparator

the device is placed in vaginal fornix by the midwife for maximum 24 hours. If Propess ® is fallen before the first 12 hours, another one could be introduce if the cervix stayed unfavourable.

After 24 hours, it is removed. If they are any contraction, oxytocin is started with or without epidural analgesic.

干预措施: Propess® (dinoprostone) (Drug)

结局指标

主要结局

Time between the beginning of the induction of labor and the delivery

时间窗: at day 1

次要结局

  • Rate of delivery hemorrhage(at day 1)
  • Rate of delivery in the first 24 hours(at day 1)
  • Application time of Cook® balloon(at day 1)
  • Time between labour induction and vaginal delivery(at day 1)
  • Bischop score when Cook balloon is fallen or retry(at day 1)
  • Time limits between the PROM and the beginning of induction(at day 1)
  • Application time of Propess®(at day 1)
  • Rate of anomaly of fetal heart rate leading stop of dinoprostone(at day 1)
  • Rate of balloon present after 12 hours(at day 1)
  • Rate of vaginal delivery with and without extraction(at day 1)
  • Rate of cesarean(at day 1)
  • Rate of epidural analgesia(at day 1)
  • Time to obtain active labour(at day 1)
  • Time to obtain complete cervix dilatation(at day 1)
  • Rate of fever during the labour(at day 1)
  • Rate of uterine hyperkinesias(at day 1)
  • Rate of clinic chorio-amnionitis defined by Newton criteria(at day 1)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (1)

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