Vaginal Microbiome Seeding and Health Outcomes in Cesarean-delivered Neonates.

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age0-50
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)

About this trial

Neonates delivered by scheduled Cesarean Section will be randomized to receive vaginal seeding (exposing the infant to Mother's vaginal flora) or sham. Infants will be followed for three years to examine health outcomes including microbiome development, immune development, metabolic outcomes, and any adverse events.

Eligibility criteria

Qualifiers

Scheduled for cesarean delivery at ≥ 37 weeks

Pregnant with single fetus, in good general health, age 18 years or older

Negative maternal testing for infections transmitted through vaginal and/or other body fluids performed as standard of care tests in early pregnancy

Negative testing for Group B strep at 35-37 weeks gestation

Disqualifiers

Delivery at a hospital other than Inova Health System

Cesarean delivery scheduled for active infection that would have interfered with vaginal delivery such as genital herpetic lesions

Rupture of membranes prior to scheduled cesarean delivery

Bacterial vaginosis within 30 days of cesarean delivery

Trial design

Treatments tested in this trial

  • Vaginal Seeding
  • No Vaginal Seeding

Treatment groups

600 Participants
are divided into 2 treatment groups

Sponsors and collaborators

National Institute of Allergy and Infectious Diseases (NIAID)

Lead sponsor

Johns Hopkins University

Collaborator

Rutgers University

Collaborator

Inova Health Care Services

Collaborator