EligibleTrials

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

Recruiting · NCT03298334 · Interventional (participants receive a specific treatment) · Lead sponsor: National Institute of Allergy and Infectious Diseases (NIAID)

View the official record on ClinicalTrials.gov →
Obesity

Interventions studied

No Vaginal SeedingVaginal Seeding

What this trial is about

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.

Who can take part

Age range
0 Days to 50 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Phase 1, Phase 2
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed across 1 US state.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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