Inova Health System
Falls Church, Virginia, 22042, United States
Location status: Recruiting
Location contact
Ankit Shah, MD
SUB_INVESTIGATOR
General Information
CONTACT
Suchitra Hourigan, MD
CONTACT
NCT Number: NCT03298334
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.
Interested in participating?
Request Info0 day–50 year
All sexes
Interventional
Phase 1 / Phase 2
Falls Church, Virginia, 22042, United States
Location status: Recruiting
Ankit Shah, MD
SUB_INVESTIGATOR
General Information
CONTACT
Suchitra Hourigan, MD
CONTACT
Cesarean section (CS) delivery is a common surgical procedure intended to increase the chances of successful delivery and to protect the health of the mother and baby. Yet this intervention is overused and has been associated with higher risk of immune and metabolic disorders in the offspring. It is hypothesized that these associations are due to CS-delivered newborns not receiving the full inoculum of maternal microbes at birth.
While restoring labor is not possible, restoring the microbes that colonize infants during birth through exposure to vaginal flora, is feasible, and has been shown in a small pilot study, to normalize the microbiota of the intestine, skin and mouth during the first month of life.
The investigators hypothesize that the restoration of the vaginal microbiota to the infant at birth will restore the infant microbiome and decrease the risk of obesity and other immune-mediated diseases linked with CS. The investigators aim to test this hypothesis in a randomized controlled trial by first examining the effect of vaginal seeding, in CS-delivered newborns, on the gut microbiota composition, structure and function (Phase I of study; first 50 infants) and then on the BMI z score and other immune-mediated outcomes (Phase II of study; 600 infants).
Methods: CS-delivered neonates will be randomized to either an experimental arm with exposure to the maternal vaginal microbiota at birth, or a control arm with no exposure. Feces, skin, saliva, breast milk, and vaginal swabs will be collected for microbiome analysis. The investigators will obtain clinical information from in-person visits, surveys and the electronic health record.
Implications: this randomized controlled clinical study will provide evidence of whether the "vaginal seeding" procedure can safely transfer microbes from mom-to-baby, and whether these microbes are beneficial for the metabolic and immune health of the child.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for Mother:
Inclusion criteria
for Infant:
[*] Standard neonatal resuscitation may include: tactile stimulation, bulb suction, oxygen without positive pressure, or drying
Exclusion criteria
for Mother:
A gauze containing the Mother's vaginal flora will be swabbed over the face and body of the neonate shortly after cesarean delivery.
A gauze carrying sterile saline will be swabbed over the face and body of the neonate shortly after cesarean delivery.
Time frame: 2 years
E.g. Body mass index z-score
Time frame: 3 years
Monitoring for adverse events
Time frame: 3 years
Intestinal microbiota development over the first three years of life
Time frame: 3 years
E.g. Monitoring for immune and inflammatory mediated conditions
Contact information is provided by the study sponsor or research team.
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
Vaginal Microbiome Seeding and Health Outcomes in Cesarean-delivered Neonates: a Randomized Controlled Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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