Last updated: July 26, 2024
Sponsor: Ohio State University
Overall Status: Active - Recruiting
Phase
4
Condition
Miscarriage
Treatment
Erythromycin
Ceftriaxone 1000 MG
Clarithromycin 500mg
Clinical Study ID
NCT06396078
2024H0122
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria
Admitted to the inpatient unit for expectant management of PPROM until delivery
Age ≥ 18 years with the ability to provide informed consent
Gestational age between 23 0/7 and 32 6/7 weeks
Exclusion criteria
Having received more than one dose of any prophylactic antibiotic
Suspected or confirmed infection requiring treatment with antibiotics
Allergy or contraindication to an antibiotic in either arm
Maternal immunosuppression
Study Design
Total Participants: 56
Treatment Group(s): 7
Primary Treatment: Erythromycin
Phase: 4
Study Start date:
July 18, 2024
Estimated Completion Date:
December 31, 2025
Study Description
Connect with a study center
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine
Columbus, Ohio 43210
United StatesActive - Recruiting
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