Comparing Impacts of Donor Human Milk to Formula Supplementation on the Gut Microbiome of Full-term Infants (PPDHM)
Microbial Colonization
About this trial
This is an interventional treatment trial for Microbial Colonization focused on measuring Sleep, Microbiome, Growth, Postpartum depression, Maternal anger, Breastfeeding, Self-efficacy
Eligibility Criteria
Inclusion Criteria: Gestation greater than 37 weeks (full-term) Completion of antibiotic protocol for GBS during labour Vaginal delivery Intending on breastfeeding Consent for infant to receive DHM Working understanding (proficient in reading and understanding) English Mother has provided signed and dated informed consent and authorization to use protected health information, as required by national and local regulations. In the investigator's opinion, the subject mother understands and can comply with protocol requirements, instructions, and protocol-stated restrictions, and is likely to complete the study as planned. Exclusion Criteria: Diagnosed with clinically significant major congenital malformation that will interfere with breastfeeding or growth No intention to breastfeed Receiving extended courses of antibiotics (beyond that of the IAP in labour)
Sites / Locations
- Rockyview General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Donor Human Milk
Standard Care (Infant Formula)
Infants randomized to the intervention group will receive DHM each time supplementation is required for the first 7 days of life.
Infants randomized to the standard care group will receive formula each time supplementation is required for the first 7 days of life.