Tearing of Membranes Before Birth - a Comparison Between Two Ways of Induction of Labor Pitocin Opposite Prostaglandin
Overview
- Phase
- Phase 3
- Intervention
- Intravenous oxytocin
- Conditions
- Fetus or Newborn or Maternal; Effects of Induction of Labor
- Sponsor
- Tel-Aviv Sourasky Medical Center
- Enrollment
- 1200
- Primary Endpoint
- The duration from the beginning of labor induction until delivery
- Last Updated
- 9 years ago
Overview
Brief Summary
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.
Detailed Description
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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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
Arms & Interventions
Intravenous oxytocin
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.
Intervention: Intravenous oxytocin
vaginal prostaglandin
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.
Intervention: vaginal prostaglandin
Outcomes
Primary Outcomes
The duration from the beginning of labor induction until delivery
Time Frame: 5 days
Secondary Outcomes
- Duration of labor induction from rupture of membranes until delivery.(5 days)