Safety and Tolerability of Lactoferrin in Very Low Birth Weight Infants



Status:Recruiting
Conditions:Obesity Weight Loss, Women's Studies
Therapuetic Areas:Endocrinology, Reproductive
Healthy:No
Age Range:Any
Updated:4/21/2016
Start Date:April 2016
End Date:March 2017
Contact:David A Kaufman, MD
Email:dak4r@virginia.edu
Phone:4349245428

Use our guide to learn which trials are right for you!

To evaluate the safety and tolerability of three different lactoferrin doses in preterm
infants

Aim1: To evaluate the safety and tolerability of three different lactoferrin doses in
preterm infants

1. Lactoferrin related adverse events and serious adverse events

2. Number of infants reaching full feeds while receiving lactoferrin (120 ml/kg/day)

3. Episodes of not receiving enteral feedings for > 24 hours once feeding is initiated

Aim 2: To evaluate lactoferrin absorption and excretion.

1. Examine lactoferrin levels in saliva, urine, plasma and stool

2. Examine lactoferrin levels in maternal and human donor milk.

Aim 3: To evaluate the effect of lactoferrin on the intestinal microbiome structure.

Inclusion Criteria:

- < 15 days of age and receiving enteral feedings

- < 1500 grams birth weight

- <37 weeks gestation

Exclusion Criteria:

- Congenital bowel obstruction ( esophageal, duodenal, small bowel or anal atresias,
Hirschsprung disease, malrotation)

- Known necrotizing enterocolitis or bowel perforation
We found this trial at
2
sites
Charlottesville, Virginia 22932
Phone: 434-924-5428
?
mi
from
Charlottesville, VA
Click here to add this to my saved trials
Charlottesville, Virginia 22908
Principal Investigator: David Kaufman, MD
Phone: 434-924-9114
?
mi
from
Charlottesville, VA
Click here to add this to my saved trials