Improvement of PPROM Management With Prophylactic Antimicrobial Therapy (iPROMPT)

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

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.

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

Preterm prelabor rupture of membranes (PPROM) is the most common identifiable risk factor associated with preterm birth and affects 1 in 3 pregnant individuals in the United States with spontaneous preterm birth. Individuals diagnosed with PPROM who meet criteria for expectant management are currently admitted to the hospital for observation until delivery, which is generally recommended at 34 weeks' gestation unless indicated sooner. Initially upon admission, a course of prophylactic antibiotics is administered as this has been shown to prolong pregnancy and improve neonatal outcomes. The standard antibiotic regimen, primarily based on data published in 1997, includes ampicillin followed by amoxicillin with erythromycin or azithromycin for a total of 7 days. Ongoing studies are needed to determine the optimal prophylactic antibiotic regimen given changes in bacterial sensitivities over time, lack of adequate coverage for common organisms including genital mycoplasma, inadequate placental transfer of currently used antibiotic agents, ineffective antibiotic response at reducing the fetal inflammatory response, and new promising antibiotic agents that address these limitations. A promising expanded-spectrum alternative regimen with proof-of-concept is ceftriaxone, clarithromycin, and metronidazole. Observational studies have shown successful eradication of intraamniotic inflammation/infection using this new regimen. This regimen offers multiple potential advantages, including: higher bioavailability, higher transplacental transfer, and effectiveness against genital mycoplasma (clarithromycin), greater anaerobic coverage (metronidazole), and a longer half-life and expanded coverage against gram-negative bacteria (ceftriaxone) compared with the current standard regimen.

Connect with a study center

  • The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine

    Columbus, Ohio 43210
    United States

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.