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Feeding Tolerance in Preterm Infants: Randomized Trial of Bolus Feeding Every 4 Hours Versus Every 3 Hours

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Urogenital Diseases+3

+ Female Urogenital Diseases and Pregnancy Complications

+ Obstetric Labor Complications

+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: February 2007
See protocol details

Summary

Principal SponsorWeill Medical College of Cornell University
Study ContactAnita G Stola, MDMore contacts
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2007

Actual date on which the first participant was enrolled.

In premature infants feeding tolerance is limited due to immaturity of gastrointestinal tract. Motor patterns of the gastrointestinal tract differ greatly in preterm infants as compared to adults. These differences in gastrointestinal motor function in premature neonates translates into less efficient gastric emptying and slower intestinal transit time. It usually manifests as residual feeds in the stomach prior to the next scheduled feeding and may be associated with abdominal distention, bile-staining aspirates, or lack of stooling. In most instances the gastric residuals are benign and relate to immature gastrointestinal motility, however they may also be an early indication of bowel obstruction, ileus or necrotizing enterocolitis. Thus, feeding intolerance often leads to temporary cessation of feeds, and prolongs the time to reach full feeds, as well as the time on parenteral nutrition (which predisposes the infants to nosocomial infection, hepatic dysfunction), and prolonged hospitalization. Achievement of adequate enteral nutrition, as soon as possible after birth is the ultimate goal for all low birth weight infants (<1250 gm); however the best methods by which sufficient enteral nutrition can be provided remain controversial. A number of feeding strategies are practiced. In our Neonatal ICU feeds are initiated by boluses and infants are being fed either every 3 hours or every 4 hours. A review of the literature (2006) revealed that there was no study comparing those two methods of feeding. We hypothesize that very low birth weight infants (≤1250 gm) will tolerate feedings better when introduced every 4 hours instead every 3 hours, by providing sufficient time for gastric emptying. We propose to conduct this prospective, randomized, clinical trial to determine whether intermittent bolus gavage feedings every 4 hours leads to better feeding tolerance than intermittent bolus gavage feedings every 3 hours in very low birth weight infants < 1250grams birth weight. Primary Hypothesis: Very low birth weight infants fed by intermittent bolus gavage every 4 hours will achieve full enteral feeding (120 kcal/kg per day) at an earlier postnatal age and have less feeding intolerance than infants fed every 3 hours. Secondary Hypothesis: Intermittent bolus gavage feeding every 4 hours will improve feeding tolerance, cause less need for parenteral nutrition and its major complication - cholestasis. Study Design: * Prospective, randomized clinical study with recruitment at NY Presbyterian Hospital Cornell Medical Center. * Written informed consent will be obtained from one or both parents prior to enrollment of each patient. Primary study endpoint: * Days to reach full feeds of 120 ml/kg per day * Incidence of feeding intolerance Secondary study endpoint: * Days on parenteral nutrition (parenteral nutrition is discontinued when an infant tolerates enteral feeding of 100 ml/kg per day). * Incidence and severity of cholestatic jaundice. Primary objective: To determine whether infants fed by intermittent gastric bolus gavage every 4 hours will have less feeding intolerance and reach full feeds at least 2 days earlier than infants fed every 3 hours. Secondary objectives: To determine if feeding every 4 hours will facilitate discontinuation of parenteral nutrition at an earlier postnatal age and result in less incidence of cholestasis. Inclusion Criteria Weight ≤ 1250 gm Sufficient stability to start early (day 3-5) enteral feedings Appropriate weight for gestational age Infants receiving ventilatory support and those with indwelling umbilical arterial catheters will be included Absence of major congenital malformations Infant will be withdrawn from the study for the following reasons: Parental request If feeding cannot be initiated prior to day of life 10 NEC requiring surgery Prolonged (> 3days) intolerance to the feeding regimen Treatment plan: Feeding Protocol * Infants who meet all of the above criteria will be randomly assigned using sealed opaque envelopes, to either every the 3 hour or every 4 hour feeding groups. * Nasogastric feeding will be initiated on the third to fifth postnatal day provided the infant's cardiorespiratory status is stable. * Bolus feeding over 30 to 60 min will be given as per usual clinical practice * Expressed breast milk is the nutrition of choice. If not available Premature Formula of 24 kcal/30 ml will be used as per usual clinical practice. * Feeding will be started and advanced in daily increments depending on infant's weight: * 500 gm to 750 gm - 10 ml/kg per day * 751gm to 1000gm - 15 ml/kg per day * 1001 gm to 1250gm - 20 ml/kg per day * Gastric residual will be measured prefeed (every 3 or 4 hours) * All feeding-related clinical decisions (when to withhold feedings) will be up to the attending physician's discretion. * Parenteral nutrition, including lipid emulsion, will be started on days 1 or 2 and continued until each infant tolerates enteral feeding of 100 ml/kg per day. * Successful achievement of full enteral feeding is defined as the ability to tolerate enteral feedings of 110-120 ml/kg per day for at least 48 hours. * Daily weight, intake and output, number of stools, number of guaiac positive stools, number of hours that feedings were withheld, episodes of apnea and bradycardia will be recorded.

Official TitleFeeding Tolerance in Preterm Infants: Randomized Trial of Bolus Feeding Every 4 Hours Versus Every 3 Hours
NCT00450697
Principal SponsorWeill Medical College of Cornell University
Study ContactAnita G Stola, MDMore contacts
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

160 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsObstetric Labor ComplicationsObstetric Labor, PrematurePregnancy ComplicationsPremature Birth

Criteria

5 inclusion criteria required to participate
Weight ≤ 1250 gm

Sufficient stability to start early (day 3-5) enteral feedings

Appropriate weight for gestational age

Infants receiving ventilatory support and those with indwelling umbilical arterial catheters will be included

Show More Criteria

4 exclusion criteria prevent from participating
Parental request

If feeding cannot be initiated prior to day of life 10

NEC requiring surgery

Prolonged (> 3days) intolerance to the feeding regimen

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

New York Presbyterian Hospital; Weill Cornell Medical College; Department of Pediatrics; Division of Neonatology

New York, United StatesOpen New York Presbyterian Hospital; Weill Cornell Medical College; Department of Pediatrics; Division of Neonatology in Google Maps
SuspendedOne Study Center
Feeding Tolerance in Preterm Infants: Randomized Trial of Bolus Feeding Every 4 Hours Versus Every 3 Hours | PatLynk