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Early Exclusive Enteral Nutrition in Early Preterm Infants

Early Exclusive Enteral Nutrition in Stable Preterm Infants at 30 0/7 - 33 6/7 Weeks Gestation: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03708068
Enrollment
69
Registered
2018-10-16
Start date
2019-04-16
Completion date
2024-01-30
Last updated
2024-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Enteral Nutrition

Keywords

Exclusive, Enteral Nutrition, Preterm Infant

Brief summary

Enteral nutrition in preterm infants is usually started and advanced slowly until reaching full enteral feeds. Most preterm infants born before 34 weeks gestation require parenteral fluids to maintain normal blood sugar level and prevent excessive weight loss and dehydration. Availability of donor human milk (DHM) along with low incidence of necrotizing enterocolitis (NEC) in preterm infants born at 30-33 weeks have encouraged neonatologists to start feeding early and advance it faster in order to shorten time on parenteral nutrition (PN) and minimize the need for intravenous access. The objectives of this trial is to study whether exclusive enteral nutrition from day of birth (i.e. no PN) results in shorter time to achieve full enteral feed when compared with traditional feeding regimen that involves a combination of PN and progressive enteral feeding.

Detailed description

Early nutritional support of preterm infants born at 30-33 weeks gestation is usually achieved via a combination of parenteral nutrition (PN) and enteral feeding that is advanced over few days to reach full enteral feed. Recent studies suggest that rapid increase of enteral feed volumes results in shorter duration on PN and earlier achievement of full enteral feed without increasing the risk of necrotizing enterocolitis (NEC) or death. Although PN has an important role in nutrition of preterm infants, it is associated with increased risk of metabolic and infectious complications even when it is used for a short period of time. Furthermore, PN mandates the need for peripheral or central intravenous access. Provision of full enteral feed volume that meets reference daily fluid intake from day of birth is used frequently and successfully in stable preterm infants born after 33 weeks. Expanding the use of this regimen to stable preterm infants born at 30-33 weeks gestation may help avoid unnecessary start of intravenous access, prevent complications related to PN, and encourage mother-infant bonding experience.

Interventions

OTHEREarly exclusive enteral nutrition

Infants will be fed at least 80% of reference daily fluid intake from day one. Feeds will be advanced by 20-30 ml/kg per day on second day onwards to meet reference daily fluid intake until infant reaches full enteral feed.

Sponsors

Belal Alshaikh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 48 Hours
Healthy volunteers
No

Inclusion criteria

1. Preterm infants born at 30 0/7 - 33 6/7 weeks gestation 2. Birth weight greater than 1000 g 3. Consent to use donor human milk 4. Postnatal age is less than 48 hours from birth 5. Infant is ready to start on feeding (as per clinical team) or feeding volume, when already started, is ≤12 ml/kg per day (total) and/or the infant received ≤2 feeds based on current feeding policy or physician descrition (total volume of the received feeds is ≤20 ml/kg per day).

Exclusion criteria

1. Cord PH \< 7.00 or Cord base access (BE) \< -16 2. Apgar score \< 7 at 5 minute 3. Lactate level ≥3 (if done for clinical indication) 4. Need for positive pressure ventilation (PPV) for \>1 minute. 5. Hemodynamic instability (hypotension or poor perfusion at any time in this 48 hours) 6. Small for gestational age \<3 percentile on Fenton chart and/or fetal absent or reversed umbilical arterial end-diastolic blood flow. 7. Major congenital malformation 8. Symptomatic or severe hypoglycemia (blood glucose \<1.8 mmol/L) 9. Infants with moderate to severe respiratory distress.

Design outcomes

Primary

MeasureTime frameDescription
Duration to achieve of full enteral feeds in daysTill 30 days of lifeDay of life to achieve full enteral feeding defined as 140 ml/kg/day which is sustained for at least 3 days

Secondary

MeasureTime frameDescription
Length of hospital stayAt discharge from neonatal intensive care unit (NICU), up to 90 days of lifeLength of hospital stay in days
Feeding intoleranceTill 30 days of lifePresence of one or more of the following: 1. vomiting more than 2 times during any 24 h period, 2. any episode of bile- or blood-stained vomiting, 3. abdominal wall erythema or tenderness that resulted in cessation of feed.
Incidence of late onset sepsisAt discharge from NICU, up to 90 days of lifeAny microbial growth in blood, cerebrospinal fluid or urine after 72 hours of admission in NICU
Incidence of NECAt discharge from NICU, up to 90 days of lifeAny Stage II and above according to Bell's staging criteria
Incidence of hypoglycemiaTill 30 days of lifeDefined as point of care testing Glucose \< 2.6 mmol/L at any time after rollment in study

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026