This study will examine the safety and tolerability of supplementation with bovine lactoferrin with fructo-oligosaccharide a simple sugar in very low birth weight infants. Lactoferrin is a major whey protein in mother's milk and plays a role in promoting a mature and healthy gut. It also has antimicrobial and immunomodulation activities.
Aim 1: To evaluate the safety and tolerability of three different lactoferrin/FOS doses in preterm infants 1. Lactoferrin/FOS related adverse events and serious adverse events 2. Time reaching full feeds while receiving lactoferrin/FOS (120 ml/kg/day) 3. Episodes of not receiving enteral feedings for \> 24 hours once feeding is initiated Aim 2: To evaluate lactoferrin/FOS absorption and excretion 1. Examine lactoferrin/FOS levels in saliva, urine, plasma, and stool 2. Examine lactoferrin levels in materal and human donor milk Aim 3: To evaluate the effect of lactoferrin/FOS on the intestinal microbiome structure
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Bovine Lactoferrin/FOS 100mg/ml dissolved in sterile water
Definitely related study solution serious adverse event
Time frame: 30 days while receiving study solution
Day after birth to reach 120ml/kg of enteral feeds
Time frame: 30 days while receiving study solution
Number of days not receiving any feedings after lactoferrin/FOS administration
Time frame: 30 days while receiving study solution
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.