drugset / Trial / NCT07563504

PROMab Trial: Ampicillin With or Without Gentamicin for Term Prelabour Rupture of Membranes

NCT07563504

Phase 4 Not yet recruiting 320 enrolled Sarawak General Hospital
RandomizedParallel-groupSingle-blindPrevention

Summary

The goal of this clinical trial is to learn whether adding gentamicin to standard ampicillin prophylaxis can better prevent clinical chorioamnionitis and other maternal and neonatal infectious complications in pregnant women aged 18 years or older with singleton, cephalic, term pregnancies and confirmed prelabour rupture of membranes. The main questions it aims to answer are: Does ampicillin plus gentamicin reduce the incidence of clinical chorioamnionitis compared with ampicillin alone? Does ampicillin plus gentamicin improve maternal infectious outcomes and neonatal infection-related outcomes compared with ampicillin alone? Researchers will compare ampicillin alone with ampicillin plus gentamicin to see whether broader antibiotic coverage reduces maternal and neonatal infectious morbidity. Participants will: 1. undergo screening and eligibility assessment 2. provide written informed consent before randomisation 3. be randomly assigned to receive either intravenous ampicillin alone or intravenous ampicillin plus gentamicin 4. start study antibiotics at 12 hours after membrane rupture and continue treatment until delivery 5. undergo routine maternal and fetal monitoring during labour and delivery have maternal and neonatal outcomes assessed during hospital stay and up to 42 days postpartum, including telephone follow-up at Day 14 and Day 42 6. optionally consent to placental tissue collection for microbiological culture at delivery

Timeline

Start
2026-07-01
Primary completion
2027-01-31
Completion
2027-03-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Gentamicin Small molecule 5 mg/kg Intravenous
Comparator Ampicillin Unknown 1 g Intravenous

Indications

No indication recorded.