跳至主要内容
临床试验/NCT02720978
NCT02720978Unknown3 期

Tearing of Membranes Before Birth - a Comparison Between Two Ways of Induction of Labor Pitocin Opposite Prostaglandin

Tel-Aviv Sourasky Medical Center0 个研究点目标入组 1,200 人开始时间: 2016年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
1,200
主要终点
The duration from the beginning of labor induction until delivery

研究概览

简要总结

Premature rupture of membranes (PROM) is a common occurrence that occurs in the incidence of 8-10% of births. Since the duration until delivery is important in avoiding the risk of complications, several studies have been performed in order to understand what is the preferred way to manage this condition of PROM in women that are not in active labor. In the largest random study that has been performed 20 years ago, there was found an advantage for labor induction with oxytocin over labor induction with Prostaglandin or waiting. However, the most important component - the BISHOP score, that affects the decision of the labor induction way, was not reported and was not taken into consideration.

详细描述

Premature rupture of membranes (PROM) is a common occurrence that occurs in the incidence of 8-10% of births. Since the duration until delivery is important in avoiding the risk of complications, several studies have been performed in order to understand what is the preferred way to manage this condition of PROM in women that are not in active labor. In the largest random study that has been performed 20 years ago, there was found an advantage for labor induction with oxytocin over labor induction with Prostaglandin or waiting. However, the most important component - the BISHOP score, that affects the decision of the labor induction way, was not reported and was not taken into consideration.

Therefore, the aim of the study is to compare randomly the perinatal outcomes in women with PROM and low BISHOP between women who undergo labor induction with Oxytocin and women who undergo labor induction with Prostaglandin E2.

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 42 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • rupture of membranes in BISHOP score lower than
  • Pregnancy week 34+0 and onward.
  • Singleton pregnancy.
  • Verifying fetal monitoring.
  • Normal maternal temperature (lower than 37.8)
  • Without vaginal bleeding or suspected placental separation
  • Contractions in frequency of less than 3 in 10 minutes
  • Signed consent form.

排除标准

  • Multiple pregnancy.
  • Maternal age below 18 or over
  • Active labor
  • Contractions in frequency of more than 3 in 10 minutes or cervical dilation ≥2 cm.
  • Lack of consent to participate in the study

研究组 & 干预措施

Intravenous oxytocin

Experimental

Women that arrive to women's ER and diagnosed with rupture of membranes in week 34+0 and onward, are not in active labor and with Bishop score lower than 7.

Those who agreed to participate in the study after signing an informed consent form will undergo the following steps:

  1. Verification rupture of membranes and gestational age.
  2. Choosing the treatment group Intravenous oxytocin from red envelope, randomly.
  3. Collecting basic and obstetric data, laboratory results and physical examination, monitoring and sonar.
  4. Induction according to departmental protocol of each delivery way.
  5. Data collecting after the delivery.

干预措施: Intravenous oxytocin (Drug)

vaginal prostaglandin

Experimental

Women that arrive to women's ER and diagnosed with rupture of membranes in week 34+0 and onward, are not in active labor and with Bishop score lower than 7.

Those who agreed to participate in the study after signing an informed consent form will undergo the following steps:

  1. Verification rupture of membranes and gestational age.
  2. Choosing the treatment group vaginal prostaglandin from red envelope, randomly.
  3. Collecting basic and obstetric data, laboratory results and physical examination, monitoring and sonar.
  4. Induction according to departmental protocol of each delivery way.
  5. Data collecting after the delivery.

干预措施: vaginal prostaglandin (Drug)

结局指标

主要结局

The duration from the beginning of labor induction until delivery

时间窗: 5 days

次要结局

  • Duration of labor induction from rupture of membranes until delivery.(5 days)

研究者

申办方类型
Other Gov
责任方
Sponsor

相似试验