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Balloon catheter versus misoprostol for the induction of labor following pre-labor rupture of membranes at term

Induction of labor with a balloon catheter versus oral misoprostol following term pre-labor rupture of membranes – a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10972090
Enrollment
650
Registered
2021-02-05
Start date
2021-02-01
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature rupture of membranes with the onset of labor more than 24 hours following rupture, prolonged rupture of membranes at term with an unfavorable cervix Pregnancy and Childbirth Premature rupture of membranes with the onset of labor more than 24 hours following rupture

Interventions

Randomization is performed by computer-sequenced block randomization technique in a two-step process, part A and B. Patients are randomized in part A into the method of cervical priming (balloon cathe

Sponsors

Helsinki University Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Aged =18 years 2. Primiparous or multiparous women with singleton pregnancy 3. Gestational age =37 weeks (term) 4. Spontaneous rupture of membranes without the onset of labor within 18-48 h 5. Unfavorable cervix (Bishops score <6) 6. Cephalic presentation of fetus 7. No colonization of Group B Streptococcus on vaginal and rectal swab

Exclusion criteria

Exclusion criteria: 1. Pre-term pre-labor rupture of membranes (<37 gestational weeks) 2. Clinical signs of infection (such as vaginitis, chorionamnionitis) 3. Active infection or carrier of human immunodeficiency virus (HIV), hepatitis B, or hepatitis C 4. Type 1 diabetes 5. Group B Streptococcal colonization of vagina and/or rectum (detected by swab test) 6. Any acute condition, maternal or fetal, requiring the immediate delivery of the fetus 7. Intrauterine growth restriction 8. Macrosomia or weight estimation =4.5 kg 9. Fetus in any other presentation than cephalic (such as breech or transverse) 10. Previous caesarean section or any other uterotomy (such as myomectomy) 11. Insufficient understanding or language deficiency to comprehend the patient guide and consent form 12. Refusal of participation or refusal for signed consent

Design outcomes

Primary

MeasureTime frame
1. Incidence of different modes of delivery (vaginal birth, assisted vaginal birth, or caesarean section), maternal infection, and newborn infection collected from patient records between hospital admission and discharge

Secondary

MeasureTime frame
1. Maternal complications of delivery (such as retention of placenta, hemorrhage, birth canal tears, and intrapartum or postpartum infection) collected from patient records between hospital admission and discharge 2. Primary assessment of the newborn measured using Apgar score at 1 and 5 min after birth, and using umbilical vein pH and base excess, need for intubation, and need for NICU admission collected from patient records between hospital admission and discharge 3. Birth experience measured using the Childbirth Experience Questionnaire (CEQ2) completed within 1 month after delivery

Countries

Finland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 5, 2026