Objective
To determine which antibiotic regimen given to pregnant women and people with preterm prelabour rupture of membranes (PPROM) is best at improving health outcomes for preterm infants.
Who will be eligible?
Pregnant women and people with preterm, prelabour rupture of membranes (PPROM) who meet the eligibility criteria and are receiving care at a hospital taking part in this trial.
Why is this important?
Preterm prelabour rupture of membranes (PPROM) is when a pregnant woman or person’s waters break early. Approximately 30-40% of women who go on to have a preterm birth experience PPROM. PPROM can lead to infections and other complications in mother and baby.
Antibiotics are routinely given to pregnant women and people who experience PPROM to reduce the risk of infection.
Why are we doing this study?
The antibiotics given after PPROM vary in Australia, Aotearoa New Zealand and worldwide. Evidence for some of these antibiotics is now quite old, and there is potential in other antibiotics that are already being used for this purpose.
PROMOAT will assess three common antibiotic regimens given after PPROM in Australia and Aotearoa New Zealand, to reduce uncertainty and understand which antibiotic is best in reducing the risk of infection in mother and baby.
Funder: NHMRC and MRFF
Ethics Reference: [Pending]
Trial Registration: [Pending]
Lead Investigators: Associate Professor Clare Whitehead and Professor Katie Groom