Premature Birth of Newborn Clinical Trial
Official title:
Extensively Hydrolyzed Liquid Human Milk Fortifier Versus Liquid Human Milk Fortifier With Supplemental Liquid Protein
Breast milk is readily accepted as the ideal source of nutrition for almost all infants, including premature or very low birth weight infants. However, these high-risk infants require the addition of fortifiers to their milk in order to achieve sufficient levels of calories, vitamins, and minerals for adequate growth. We are currently using a liquid human milk fortifier which does not provide sufficient protein intake, requiring addition of a liquid protein supplement. A new product has been released which provides sufficient protein in the liquid HMF, without the acidification seen in previous products. This is a prospective, randomized noninferiority study comparing the safety and efficacy of the new HMF with additional protein to our current standard of adding additional protein supplementation on top of the HMF.
All infants admitted to the Neonatal Intensive Care Unit (NICU) at Cardinal Glennon at gestational age <32 weeks and birthweight <1500g, and whose mothers intend to use breast milk (maternal or donor) will be approached for study participation. Infants can be enrolled at any point up until their feedings become fortified, typically around the 8th day of life. Eligible infants whose parents consent for participation will be randomized to one of the two study regimens. Sealed envelopes containing the subject treatment group will be prepared from randomization schedules that are computer-generated using a pseudorandom permuted blocks algorithm. Multiples will be randomized together to the same treatment group. The randomization will be block stratified by birth weight (500-1000g and 1001-1500g). Infants will have laboratory values to follow for signs of metabolic acidosis and nutritional status. These labs (BMP, Magnesium, Phosphorous, Alkaline Phosphatase, and prealbumin) will be drawn on study days 1, 15, and 30. Total blood volume for these labs is approximately 1.4 mL, and may be obtained by venipuncture or heel stick. These labs are monitored for nutritional sufficiency in very low birth weight infants already, the only change will be the timing that the labs are obtained. Infants will remain on their designated HMF until one of 3 different time points: 1) Infant does not tolerate HMF and must be taken off, 2) Infant is no longer receiving breastmilk and is transitioned to a premature formula, or 3) Infant is getting ready to go home and HMF is removed from the feedings. Hospitalization data will be collected on the infants until they are either discharged from the NICU or until they reach 36 weeks corrected gestational age, whichever occurs first. Data collected will include: birthweight, gestational age, gender, antenatal steroids, APGARs, days of parenteral nutrition, day enteral feedings were initiated, daily enteral volume intake, daily caloric and protein intake, day of HMF and/or liquid protein initiation. Lab data will be recorded as noted above. Growth data will be recorded by daily weights and weekly head circumferences and lengths. Intolerance will be assessed by incidence of feeding intolerance, nil per os (NPO) time, change in diet due to intolerance, incidence of metabolic acidosis, incidence of necrotizing enterocolitis, incidence of spontaneous intestinal perforation, cause of death, and length of hospital stay. Data on NICU complications, including late onset sepsis, retinopathy of prematurity, intraventricular hemorrhage, bronchopulmonary dysplasia, and use of postnatal steroids (which can affect growth) will also be recorded. Neurodevelopmental data will be collected on the infants from their first Bayley evaluation in the Nursery Follow-up clinic, usually performed at 15-18 months of age. We will record cognitive, language, and motor scores. We will also collect information on therapy services received, and incidence of blindness or deafness. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT02452580 -
The Norwegian Family Centered Care Study
|
||
Completed |
NCT02502916 -
Enteral Feeding and Early Gut Colonization of Preterm Infants
|
N/A | |
Completed |
NCT01748214 -
Premature Infant Exposure to Noise Generated by Respiratory Support
|
N/A | |
Terminated |
NCT02840825 -
Biochip for HCMV Detection in Breast Milk
|
||
Recruiting |
NCT02306317 -
The Adding Value of Parents to Nursing Care in the Control of FiO2
|
N/A | |
Completed |
NCT01354028 -
Effects of Massage Therapy to Induce Sleep in Preterm Infants
|
N/A | |
Completed |
NCT01881256 -
The BabyGrow Longitudinal Study of Nutrition and Growth in Preterm Infants
|
N/A | |
Completed |
NCT02788786 -
Feasibility and Acceptability of Use of Daily Oral Rinse in Pregnant Women in Rural Nepal
|
Phase 2 | |
Completed |
NCT01678638 -
Timing of Inguinal Hernia Repair in Premature Infants
|
N/A | |
Recruiting |
NCT02623400 -
The Effect of Perinatal Stress on the Development of Preterm Infants
|
||
Completed |
NCT02523222 -
Prophylactic Dextrose Gel for Newborns at High-risk for Hypoglycemia
|
N/A | |
Active, not recruiting |
NCT02508571 -
Direct Swallowing Training and Oral Sensorimotor Stimulation in Preterm Infants
|
N/A | |
Completed |
NCT02478684 -
Delayed Cord Clamping in Preterm Neonates
|
N/A | |
Completed |
NCT02477423 -
A Randomized Controlled Trial Investigating if Antibiotic Use in the First 48 Hours of Life Adversely Impacts the Preterm Infant Microbiome
|
N/A | |
Terminated |
NCT02040909 -
Optimizing Propofol Dosing for (Preterm) Newborn Infants That Need Endotracheal Intubation
|
Phase 1 | |
Completed |
NCT00722943 -
Neuroendocrine Mechanisms of Developmental Massage Therapy (DMT) in Preterm Infants: Clinical Study
|
N/A | |
Active, not recruiting |
NCT02832011 -
How Effect Olive Oil and Eoprotin on Immunological Parameters and Growth
|
N/A | |
Completed |
NCT02643472 -
GPS (Giving Parents Support): Parent Navigation After NICU Discharge
|
N/A | |
Terminated |
NCT01759134 -
Comparison of Post-Discharge Growth of Premature Infants Using Two Different Formulas
|
Phase 4 | |
Completed |
NCT01628510 -
The Developmental Effects of NICU Positioning
|
N/A |