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Balloon + Oxytocin Versus Oral Misoprostol to Induce Labor in Case of PROM (RUBAPRO2)

Phase 4
Recruiting
Conditions
Cervical Ripening
Premature Rupture of Fetal Membranes
Induction of Labor
Nulliparous
Interventions
Device: Balloon for cervical ripening (Teleflex French Dufour catheter CH20 reference 174000)
Registration Number
NCT05568745
Lead Sponsor
University Hospital, Clermont-Ferrand
Brief Summary

Premature rupture of membranes (PROM) at term complicates 6 to 22% of singleton pregnancies. Spontaneous labour occurs in 60-67% of these patients within 24h. If no effective uterine contraction occurs, induction of labour (IOL) is the strategy recommended by the French as well as the American College of Obstetricians and Gynecologists. The optimal strategy for IOL in case of PROM with an unfavourable cervix remains unknown and none of the studies conducted in nulliparous women showed the superiority of one induction method over another.

In the current project, we aimed to determine (1) if IOL with association of balloon catheter and oxytocin after 6 hours could increase the rate of delivery \< 24h versus low dose of oral misoprostol (25 µg oral PGE1 every 2h) in case of PROM at term in nulliparous women and (2) patient satisfaction using EXIT survey assessed before hospital discharge.

Detailed Description

Context : Premature rupture of membranes (PROM) at term complicates 6 to 22% of singleton pregnancies. Spontaneous labour occurs in 60-67% of these patients within 24hours. If no effective uterine contraction occurs, induction of labour (IOL) is the strategy recommended by the French as well as the American College of Obstetricians and Gynecologists. The optimal strategy for IOL in case of PROM with an unfavourable cervix remains unknown and none of the studies conducted in nulliparous women showed the superiority of one induction method over another1. Oral misoprostol (ProstaglandinE1, PGE1) usually demonstrated the lowest rate of c-section after IOL in general population and balloon catheter was associated with the lowest rate of uterine hyperstimulation. Recently, a comparison 1 to 1 between these two methods was conducted in singletons with comparable results. Despite recent studies demonstrating no higher risk of infectious complications using mechanical device in the context of PROM, only prostaglandins and oxytocin are usually recommended. Recently, Devillard et al. demonstrated that the combination of balloon catheter plus oxytocin systematically infused after 6 hours increased the rate of delivery \<24h compared to dinoprostone vaginal insert group (90% versus 57.5% respectively) and decreased the time between induction and delivery in nulliparous group (17.0hours versus 26.5hours).

In the current project, we aimed to determine (1) if IOL with association of balloon catheter and oxytocin after 6 hours could increase the rate of delivery \< 24hours versus low dose of oral misoprostol (25 µg oral PGE1 every 2h) in case of PROM at term in nulliparous women and (2) patient satisfaction using EXIT (EXperience of Induction Tool) survey assessed before hospital discharge.

We hypothesized that the rate of delivery \< 24hours will be 15% higher in the group induced with balloon + oxytocin (estimated around 85 %) compared to the misoprostol group (estimated around 70 %). Patient satisfaction concerning experience of IOL will be assessed using a validated survey- the EXperience of Induction Tool (EXIT) - translated in French language (Beckman et al., 2017). We aimed to demonstrate a difference greater than an effect-size of 0.25.

Objectives: The main objective is to demonstrate higher rate of vaginal birth \<24hours by insertion of a balloon catheter + oxytocin after 6hours, versus low dose of oral misoprostol (25 µg oral PGE1 every 2hours) in case of unfavorable cervix beyond 12 hours of PROM in nulliparous and to compare patient satisfaction using EXIT survey translated in French language before hospital discharge.

The secondary objectives are:

* To compare the rate of caesarean sections in the two groups.

* To compare the safety related to women of both induction methods in terms of maternal morbidities, uterine hyperstimulation, maternal infections and other reported adverse events (AEs).

* To compare the safety related to neonates of both induction methods in terms of neonatal morbidities, neonatal infections and other reported AEs.

Study type: Multi-center, randomized, controlled, open-label therapeutic trial with two parallel arms.

Number of centers: 5

Study Description:

The study group is the balloon catheter group with addition of oxytocin as early as 6h after the catheter insertion. After 12 hours of balloon insertion, induction of labour is continued by oxytocin alone. The control group corresponds to induction with misoprostol 25µg given orally (oral prostaglandin E1). The same dose is delivered every 2 hours until labour onset with a maximum of 8 administrations. Oxytocin can be started at least 4 hours after the last misoprostol administration.

Patients will be assigned by random allocation on a 1:1 basis in permuted blocks to either treatment group or control group using a dedicated, password-protected, SSL-encrypted website. To minimize the risk of imbalance between the study groups, the randomization will be stratified by trial site.

Primary endpoint: Hierarchical primary endpoint: (1) Proportion of patients vaginally delivered \<24h and (2) patient satisfaction using EXIT survey assessed before hospital discharge.

Number of patients: 520

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
520
Inclusion Criteria
  • Age > 18 years old,
  • Pregnant, Gestational age ≥ 37 weeks
  • Singleton pregnancy with cephalic presentation
  • Nulliparous
  • PROM without labour beyond 12 hours
  • Unfavourable cervix (Bischop score < 6)
  • Able to give her informed consent
  • Ability to comply with the requirement of the study
  • Covered by the French Social Security welfare system
Exclusion Criteria
  • Unable to understand French language

  • Contraindication for vaginal delivery

  • Loss of meconium amniotic fluid (LA)

  • Temperature > 38.2°C

  • Intrauterine infection

  • IUGR with Doppler anomaly

  • Fetus with expected polymalformative syndrome

  • Scarred womb

  • Suspicion of genital herpes

  • Known HIV seropositivity

  • Placenta praevia

  • Fetal death

  • Abnormal FHR (Fetal Heart Rate)

  • Contraindication to misoprostol:

    • Allergy or hypersensibility
    • Suspicion or confirmation of a scarred uterus following past surgical intervention
    • Renal insufficiency
    • Malformation of the uterus
  • Contraindication to balloon:

    • Vasa praevia, placenta praevia
    • Invasive cervical cancer
  • Contraindication to oxytocin

    • Allergy or hypersensibility
    • Dystocia
    • Fragility or excessive distension of the uterus
    • Uterine hypertonia or fetal distress when delivery is not imminent
    • Cardiovascular disorders and severe preeclampsia
    • Predisposition to amniotic embolism (in utero fetal demise, abruption).
  • Patient subject to a legal protection order (curatorship or tutorship)

  • Refusal to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Oral misoprostolMisoprostol Oral TabletPatients will receive misoprostol 25 micrograms given orally (oral prostaglandin E1). The same dose will be given every 2 hours until beginning of labor with a maximum of 8 administrations. (Oxytocin can be started at least 4 hours after the last misoprostol administration if patient remains not in labour.)
Balloon+oxytocinBalloon for cervical ripening (Teleflex French Dufour catheter CH20 reference 174000)Mecanical cervical ripening will be done by transcervical balloon (Teleflex French Dufour catheter CH20 reference 174000). Oxytocin will be started 6 hours after balloon insertion. At H12 balloon will be removed and induction continued by oxytocin alone.
Balloon+oxytocinOxytocinMecanical cervical ripening will be done by transcervical balloon (Teleflex French Dufour catheter CH20 reference 174000). Oxytocin will be started 6 hours after balloon insertion. At H12 balloon will be removed and induction continued by oxytocin alone.
Primary Outcome Measures
NameTimeMethod
Vaginal delivery <24hoursat birth

Proportion of patients vaginally delivered \<24hours (in %)

Patient satisfactionup to 4 days

Satisfaction of women concerning method of induction by the EXperience of Induction Tool (EXIT) validated in french language.

Secondary Outcome Measures
NameTimeMethod
Mode of deliveryat birth

Rate in %

maternal-fetal infectionup to 4 days

Rate of maternal-fetal infection in %

Birth weight of the newbornat birth

in grammes

Apgar score < 75min after birth

Neonatal endpoint (yes/no)

pH umbilical arteryat birth

pH at the umbilical artery

Base defect and lactate (umbilical artery)at birth

mmol/L

Neonatal tranferup to 4 days

Rate of neonatal transfer to intensive care unit or neonatology unit

Duration from rupture to beginning of inductionat birth

in hours

Duration between IOL and deliveryat birth

in hours

Duration of balloon exposure or misoprostol exposureat birth

in hours

Misoprostol receivedat birth

Total dose of misoprostol received (in µg)

Bishop score on balloon removalat birth

(comprised between 0 and 13)

Balloon in place (yes/no)at birth

Rate of balloon in place (%) at 12 hours after the beginning of induction

Duration between induction and full cervical dilatationat birth

Duration (in hours)

Post-partum hemorrhageup to 4 days

Rate in %

Rate of feverduring labor

Rate in %

Rate of patients experiencing episode(s) of uterine hyperstimulationduring labor

Rate of patients experiencing episode(s) of uterine hyperstimulation (%) during labour (defined by the necessity to interrupt oxytocin and/or to inject pharmacological agents in the context of excessive number of contractions with or without abnormal FHR),

Endometritisup to 4 days

Rate of endometritis in %

Duration of hospital stayup to 4 days

Duration (in days)

Trial Locations

Locations (5)

CHU de Saint Etienne

🇫🇷

Saint-Étienne, France

CHU de Toulouse

🇫🇷

Toulouse, France

CHU de Clermont-Ferrand

🇫🇷

Clermont-Ferrand, France

Assistance Publique Hôpitaux de Paris- CHU Bicêtre

🇫🇷

Le Kremlin-Bicêtre, France

CHU de Bordeaux

🇫🇷

Bordeaux, France

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