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Study identifier: NCT06396078 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Improvement of PPROM Management With Prophylactic Antimicrobial Therapy (iPROMPT)

Condition: Preterm Premature Rupture of Membrane · Pregnancy, High Risk · Preterm Birth  ·  Sponsor: Ohio State University

PhasePhase 4
Planned participants56
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

To conduct an unblinded pragmatic randomized controlled trial (pRCT) "Improvement of PPROM Management with Prophylactic Antimicrobial Therapy (iPROMPT)" of a seven-day course of ceftriaxone, clarithromycin, and metronidazole versus the current standard of care of a seven-day course of ampicillin/amoxicillin and azithromycin or erythromycin to prolong pregnancy and decrease adverse perinatal outcomes among hospitalized pregnant individuals undergoing expectant management of PPROM \<34 weeks.

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

Talk to the study team

Marissa Berry, MD  ·  614-293-4780  ·  Marissa.Berry@osumc.edu

Always discuss trial participation with your own doctor first.

Locations (2)

The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal MedicineColumbus, Ohio, United StatesRecruiting
University of Texas Medical BranchGalveston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06396078