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
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