Vaginal Seeding for Cesarean Section Babies
(MOTHER SEED Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether swabbing C-section babies with their mother's vaginal fluids can safely alter the bacteria in their noses. Researchers aim to determine if this process, known as vaginal seeding, impacts the early-life respiratory health of these babies. In the trial, some babies will receive the vaginal swab, while others will receive a sterile swab (placebo swab) for comparison. Mothers planning a scheduled C-section at Vanderbilt University Medical Center and who have undergone certain prenatal screenings might be suitable candidates. As an unphased trial, this study provides a unique opportunity to contribute to groundbreaking research on newborn health.
Do I need to stop my current medications to participate in the trial?
The trial does not specify if you need to stop taking your current medications. However, it excludes participants who have used certain medications like systemic antibiotics or immunosuppressive agents shortly before delivery, so it's best to discuss your specific medications with the trial team.
What prior data suggests that vaginal seeding is safe for cesarean-born children?
Research shows that vaginal seeding is under investigation for safety in newborns. This process involves swabbing infants born via cesarean section with their mother's vaginal fluids. Studies indicate that this can alter the community of bacteria, known as the microbiome, in these babies. For example, certain bacteria like Enterobacteriaceae decrease. Although research has focused on these bacterial changes, no major safety issues have emerged. However, more studies are needed to confirm these findings.
Since detailed safety data is not yet available, the trial's "not applicable" phase suggests it is considered low-risk, as early phases usually focus on safety. Participants in such trials help researchers better understand any potential risks or benefits.12345Why are researchers excited about this trial?
Researchers are excited about the vaginal seeding technique for babies born via cesarean section because it has the potential to mimic the natural bacterial exposure that occurs during a vaginal birth. Most cesarean-born babies miss out on this initial exposure to beneficial bacteria, which can play a crucial role in developing their immune systems. By using a swab to transfer maternal vaginal fluids to the newborn, this method aims to introduce these beneficial microbes early on, possibly offering health benefits not typically available with the standard sterile environment of a cesarean delivery. This could lead to improved long-term health outcomes, such as a reduced risk of allergies and autoimmune conditions.
What evidence suggests that vaginal seeding is effective for modifying the URT microbiome in C-section babies?
Research shows that "vaginal seeding," which participants in this trial may receive, can help C-section babies develop a microbiome similar to those born naturally. This process involves gently wiping the baby with the mother's vaginal fluids. Some studies have found small changes in the gut bacteria of these babies, suggesting possible benefits. Evidence also indicates a reduction in certain bacteria, like Enterobacteriaceae, in babies who undergo this procedure. While it might not significantly affect allergy risks or growth, it is considered safe and could aid some aspects of development. Overall, more research is needed, but early results are promising for adjusting the microbiome of C-section-born babies.12356
Who Is on the Research Team?
Christian Rosas-Salazar, MD, MPH
Principal Investigator
Vanderbilt University Medical Center
Are You a Good Fit for This Trial?
This trial is for healthy infants born by C-section at VUMC, with mothers aged 18-40 intending to breastfeed and have pediatric care at VUMC. Exclusions include maternal infections like HIV or hepatitis, fever before delivery, use of certain antibiotics or immunosuppressives near delivery time, labor complications, and serious infant health issues.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Nose swabbing with either maternal vaginal secretions or a sterile swab is performed immediately after birth
Follow-up
Participants are monitored for safety and effectiveness after the intervention
What Are the Treatments Tested in This Trial?
Interventions
- Sterile Swab
- Vaginal Seeding
Find a Clinic Near You
Who Is Running the Clinical Trial?
Vanderbilt University Medical Center
Lead Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator