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Study identifier: NCT07183462 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Azithromycin and Ampicillin for Late PPROM

Condition: Pregnancy Complications, Infectious · Premature Birth · Neonatal Diseases and Abnormalities  ·  Sponsor: Sheba Medical Center

PhasePhase 4
Planned participants311
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn whether adding azithromycin to the standard antibiotic treatment (ampicillin) improves newborn outcomes in women with preterm premature rupture of membranes (PPROM) between 34.0 and 36.6 weeks of pregnancy. The main question it aims to answer is: Does the combination of ampicillin and azithromycin lower the risk of serious neonatal health problems compared to ampicillin alone? Researchers will compare two antibiotic regimens: Ampicillin alone, which is the current standard care Ampicillin with azithromycin, a broader regimen that may better prevent infections and prolong pregnancy Participants will: Receive one of the two antibiotic treatments during hospitalization. Be monitored until delivery for signs of infection and labor All participants will stay in the hospital until delivery. The study also looks at how the antibiotic choice may affect the time between membrane rupture and delivery, maternal infections, and the need for neonatal intensive care.

This description comes directly from the study's public registry record.

Talk to the study team

Noa Gonen, MD  ·  972-54-3955584  ·  gonen.noa7@gmail.com

Michal Fishel - Bartal, MD  ·  972-52-8087034  ·  michalbartal@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Sheba medical centerRamat Gan, Israel, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT07183462