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临床试验/NCT01099280
NCT01099280已完成3 期

Induction of Labor in Term Premature Rupture of Membranes: A Comparison Between Oxytocin and Dinoprostone Followed Six Hours Later by Oxytocin

Erzincan Military Hospital1 个研究点 分布在 1 个国家目标入组 225 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
225
试验地点
1
主要终点
the number (rate) of women who succeeded in delivering vaginally within 24 h of the initiation of the labor induction protocol

研究概览

简要总结

Prelabor rupture of membranes (PROM) is most commonly defined as rupture of membranes before the onset of labor and occurs in 8% of term pregnancies. A prolonged interval from rupture of membranes to delivery is associated with an increase in the incidence of chorioamnionitis and neonatal sepsis. The management of the term patients with PROM, especially those with an unfavorable cervix, remains controversial. Management options to choose from are immediate induction of labor versus delayed induction or expectant management. Several reports have detailed an increase in maternal and neonatal morbidity with expectant management, whereas active management leads to a shorter interval from PROM to delivery, reducing the risk of postnatal infections. In addition, active management is preferred by patients.

The investigators know that, neonatal intensive care admission, variable decelerations, and primary cesarean delivery rates are positively correlated with a longer admission-to-labor-onset interval in women with PROM . So, to reduce the induction to delivery times, concurrent oxytocin infusion with dinoprostone vaginal pessary use for labor induction in women with PROM may be beneficial. Several studies have shown shorter induction-to-delivery interval with concurrent oxytocin infusion with prostaglandin agent at initiation of labor . However, in these studies, there is a a paucity information in PROM labor induction. Only one randomized control trial have compared the efficacy of concurrent dinoprostone and oxytocin and oxytocin alone in women with term PROM . This study indicated that concurrent vaginal dinoprostone and intravenous oxytocin conferred no advantage over intravenous oxytocin alone for the outcomes of interest, including length of labor patient satisfaction or risk for cesarean delivery. Unfortunately, this study was limited by small sample size.

The aims of this randomized study was to compare two protocols (oxytocin vs. sustained-release dinoprostone followed six hours later by oxytocin) for induction of labour in women with PROM at term and an unfavorable cervix.

研究设计

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

  • Women with a live singleton fetus at term [37-42 weeks of gestation in cephalic presentation
  • reactive nonstress test (NST)
  • presenting with PROM
  • a Bishop score of 5 or less before the onset of labor
  • an absence of spontaneous contractions

排除标准

  • Women in active labor
  • previous uterine surgery,
  • antepartum hemorrhage,
  • chorioamnionitis,
  • contraindication to prostaglandin use (bronchial asthma, glaucoma), *contraindication to vaginal delivery,
  • multiple pregnancy,
  • non-vertex presentation
  • major fetal anomalies

研究组 & 干预措施

oxytocin group

Experimental

2 milliunits/min and doubled every 30 minutes to a maximum of 32 milliunits/min or until four contractions in 10 minutes was achieved

干预措施: SYNPITAN FORT 5 IU (Drug)

dinoprostone and oxytocin

Experimental

a single dose sustained-released dinoprostone into the posterior vaginal fornix. A standard intravenous oxytocin was administered 6 hours after the insertion of the vaginal pessary. An initial dose of 2 mU/min was increased at 30 minute intervals by 2 mU/min to a maximum dose 32 mU/min or until four contractions in 10 minutes was achieved

干预措施: Propess,SYNPITAN FORT (Drug)

结局指标

主要结局

the number (rate) of women who succeeded in delivering vaginally within 24 h of the initiation of the labor induction protocol

时间窗: 24 hours

次要结局

  • labor induction-to-delivery interval(48 hours)

研究者

发起方
Erzincan Military Hospital
申办方类型
Other

研究点 (1)

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