Is Feeding During Therapeutic Hypothermia Safe and Can Improve Outcomes in Infants With Hypoxic-ischaemic Encephalopathy: a Randomized Controlled Study.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Therapeutic hypothermia (TH) is the standard of care for newborns with moderate to severe hypoxic-ischaemic encephalopathy (HIE) born at 35 weeks or more of gestation. Many neonatal units do not use enteral feeding during TH, in fear of increased risk of complications. Withholding enteral feedings during TH lacks supporting evidence. The aim of the study is to determine if enteral feeding during TH in patients with HIE is safe and assess its effects. Investigators will perform multicenter randomized controlled study in level III neonatal intensive care units on infants qualified for TH. Infants will be randomized into 2 groups: (1) unfed during 72 hours of TH; (2) fed group, which will start receive enteral feeding with mother milk or human donor breast milk at 10 ml/kg/day during first day of TH, 20 ml/kg/day during second day, 30 ml/kg/day during third day. The primary outcome will be (1) combined necrotizing enterocolitis or death, (2) length of hospital stay. The secondary outcomes will be (1) time to full enteral feeding, (2) late-onset sepsis, (3) Test of Infant Motor Performance scoring, (4) MRI scoring, (5) MR spectroscopy parameters.

Eligibility
Participation Requirements
Sex: All
Maximum Age: Newborn
Healthy Volunteers: f
View:

• 35 weeks or more gestational age

• \< 6 hours post birth

• Any of the following:

‣ Metabolic or mixed acidosis with a pH of ≤7.0 or a base deficit ≥16 mmol/L in an umbilical cord blood sample or any blood obtained within first hour after birth

⁃ 10-minute Apgar score of ≤5

⁃ Ongoing resuscitation initiated at birth and continued for ≥10 minutes

• Moderate to severe encephalopathy on clinical examination, using a Thompson HIE score ≥ 7

• Signed informed consent by parent

Locations
Other Locations
Poland
University Children's Hospital of Cracow, Neonatal intensive care unit
RECRUITING
Krakow
Contact Information
Primary
Viktoryia Parfenchyk, MD
viktoryia.parfenchyk@uj.edu.pl
+48 535275959
Backup
Matuesz Jagla, MD
mateusz.jagla@uj.edu.pl
Time Frame
Start Date: 2024-04-15
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 104
Treatments
No_intervention: control group
Control group will be unfed orally during 72 hours of therapeutic hypothermia. The group will be receiving parenteral nutrition (PN) from day one onwards. Parenteral nutrition will be defined as receiving any type of nutrient solution in any volume through any route of administration (peripheral venous cannula, central venous catheter, or umbilical catheter).
Experimental: experimental group
Experimental group will start receiving enteral feeding at 10 ml/kg/day during first day of TH, 20 ml/kg/day during second day and 30 ml/kg/day during third day.~Additionally will be receiving parenteral nutrition (PN) from day one onwards. Parenteral nutrition will be defined as receiving any type of nutrient solution in any volume through any route of administration (peripheral venous cannula, central venous catheter, or umbilical catheter). As the volume of enteral feeding will be increased, the volume of PN will be decreased gradually.
Sponsors
Leads: Nutricia Foundation

This content was sourced from clinicaltrials.gov