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Early Progressive Feeding in Human-Milk Fed Extremely Preterm Infants: A Randomized Trial

Primary Purpose

Premature; Infant, Light-for-dates

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Progressive Feeding without MEF
Progressive Feeding with MEF
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Premature; Infant, Light-for-dates focused on measuring premature infant, early progressive feeding

Eligibility Criteria

24 Hours - 48 Hours (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • admission to the NICU within 48 hours with gestational age between 22.0 and 28.6 weeks

Exclusion Criteria:

  • small for gestational age (<10th percentile birthweight), major congenital or chromosomal anomalies, and infants with terminal illness in which decision to withhold or limit support have been made

Sites / Locations

  • University of Alabama at Birmingham

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Progressive Feeding without MEF

Progressive Feeding with MEF

Arm Description

This group will receive feeding volumes of 20-24ml/kg/d of day 1 of feeding followed by the study intervention of daily volume increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.

This group will receive minimal enteral feeds (MEF) with volumes of 20-24ml/kg/d for 4 days followed by daily increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.

Outcomes

Primary Outcome Measures

Number of days alive and receiving full enteral feeding
number of days alive on full enteral feeding in the first 28 days after birth

Secondary Outcome Measures

Number of participants with diagnosis of necrotizing enterocolitis
diagnosis of necrotizing enterocolitis stage 2 or 3
Number of participants with diagnosis of intestinal perforation
Death
death prior to 121 days of birth
Number of days alive and receiving full enteral feeding according to time of exposure to human milk and formula feeding the first 28 days
Time to establish full enteral feeding
time interval between birth and full enteral feeding at 120cc/kg/day
Number of episodes of feeding intolerance
interruption or cessation of enteral feeds for a period greater than 12 hours for abnormal abdominal examination
Number of episodes of feeding intolerance resulting in an interruption or cessation of progressive enteral feeding for a period < 12 hours
Number of days receiving parenteral nutrition
Number of days requiring central line access
Number of episodes of culture proven sepsis
Growth/length at time of discharge
Duration of hospital stay in days
Changes in intestinal microbiome
Determined by molecular analyses of bacteria in fecal samples

Full Information

First Posted
September 19, 2016
Last Updated
December 13, 2022
Sponsor
University of Alabama at Birmingham
Collaborators
The Gerber Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02915549
Brief Title
Early Progressive Feeding in Human-Milk Fed Extremely Preterm Infants: A Randomized Trial
Official Title
Early Progressive Feeding in Human-Milk Fed Extremely Preterm Infants: A Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
November 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
The Gerber Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To test the hypothesis that progressive feeding without minimal enteral feeding (MEF) compared to progressive feeding preceded by a 4-day course of MEF will result in an increased number of days alive on full enteral feeding in the first 28 days after birth in extremely preterm infants receiving human milk.
Detailed Description
Qualifying participants will be randomly assigned to one of two study groups: 1) Early progressive feeding without MEF or 2) Progressive feedings preceded by 4 days of MEF. Regardless of study group assignment, donor human milk will be offered if not enough of the mother's expressed breastmilk during the intervention phase of the trial. Intervention group: Progressive feeding of 20-24 ml/kg/d on day 1 of feeding, followed by daily increments of 24-25 ml/kg/d as tolerated until full enteral feeding achieved. Control group: MEF with feeding volumes of 20-24 ml/kg/d for 4 days followed by progressive feeding (daily increments of 24-25 ml/kg/d) as tolerated until full enteral feeding achieved. Both groups will receive fast progressive feeding (>/= 24 ml/kg/day) If parent agrees, stool "dirty" diapers will be collected 5 times (at birth, 1, 2, 3 and 4 weeks of life).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature; Infant, Light-for-dates
Keywords
premature infant, early progressive feeding

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Progressive Feeding without MEF
Arm Type
Experimental
Arm Description
This group will receive feeding volumes of 20-24ml/kg/d of day 1 of feeding followed by the study intervention of daily volume increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.
Arm Title
Progressive Feeding with MEF
Arm Type
Active Comparator
Arm Description
This group will receive minimal enteral feeds (MEF) with volumes of 20-24ml/kg/d for 4 days followed by daily increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.
Intervention Type
Other
Intervention Name(s)
Progressive Feeding without MEF
Intervention Description
This group will receive feeding volumes of 20-24ml/kg/d of day 1 of feeding followed by the study intervention of daily volume increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.
Intervention Type
Other
Intervention Name(s)
Progressive Feeding with MEF
Intervention Description
This group will receive minimal enteral feeds (MEF) with volumes of 20-24ml/kg/d for 4 days followed by daily increases in increments of 24-25ml/kg/d as tolerated until full enteral feeding is achieved.
Primary Outcome Measure Information:
Title
Number of days alive and receiving full enteral feeding
Description
number of days alive on full enteral feeding in the first 28 days after birth
Time Frame
birth to 28 days
Secondary Outcome Measure Information:
Title
Number of participants with diagnosis of necrotizing enterocolitis
Description
diagnosis of necrotizing enterocolitis stage 2 or 3
Time Frame
birth to 120 days or discharge, whichever occurs first
Title
Number of participants with diagnosis of intestinal perforation
Time Frame
birth to 14 days
Title
Death
Description
death prior to 121 days of birth
Time Frame
birth to 120 days
Title
Number of days alive and receiving full enteral feeding according to time of exposure to human milk and formula feeding the first 28 days
Time Frame
birth to 28 days
Title
Time to establish full enteral feeding
Description
time interval between birth and full enteral feeding at 120cc/kg/day
Time Frame
birth to 28 days
Title
Number of episodes of feeding intolerance
Description
interruption or cessation of enteral feeds for a period greater than 12 hours for abnormal abdominal examination
Time Frame
birth to 28 days
Title
Number of episodes of feeding intolerance resulting in an interruption or cessation of progressive enteral feeding for a period < 12 hours
Time Frame
birth to 28 days
Title
Number of days receiving parenteral nutrition
Time Frame
birth to 28 days
Title
Number of days requiring central line access
Time Frame
birth to 28 days
Title
Number of episodes of culture proven sepsis
Time Frame
birth to 120 days or discharge, whichever occurs first
Title
Growth/length at time of discharge
Time Frame
birth to 120 days or discharge, whichever occurs first
Title
Duration of hospital stay in days
Time Frame
birth to 120 days or discharge, whichever occurs first
Title
Changes in intestinal microbiome
Description
Determined by molecular analyses of bacteria in fecal samples
Time Frame
birth to 28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Hours
Maximum Age & Unit of Time
48 Hours
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: admission to the NICU within 48 hours with gestational age between 22.0 and 28.6 weeks Exclusion Criteria: small for gestational age (<10th percentile birthweight), major congenital or chromosomal anomalies, and infants with terminal illness in which decision to withhold or limit support have been made
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ariel A. Salas, MD, MSPH
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35249
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29529231
Citation
Salas AA, Li P, Parks K, Lal CV, Martin CR, Carlo WA. Early progressive feeding in extremely preterm infants: a randomized trial. Am J Clin Nutr. 2018 Mar 1;107(3):365-370. doi: 10.1093/ajcn/nqy012.
Results Reference
result
PubMed Identifier
34775476
Citation
Salas AA, Willis KA, Carlo WA, Yi N, Zhang L, Van Der Pol WJ, Younge NE, Lefkowitz EJ, Lal CV. The gut microbiome of extremely preterm infants randomized to the early progression of enteral feeding. Pediatr Res. 2022 Sep;92(3):799-804. doi: 10.1038/s41390-021-01831-w. Epub 2021 Nov 13.
Results Reference
result
PubMed Identifier
36442467
Citation
Durham L, Gunawan E, Nguyen K, Reeves A, Shukla V, Salas AA. Total Fluid Administration and Weight Loss during the First 2 Weeks in Infants Randomized to Early Enteral Feeding after Extremely Preterm Birth. Neonatology. 2023;120(2):257-262. doi: 10.1159/000527430. Epub 2022 Nov 28.
Results Reference
result

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Early Progressive Feeding in Human-Milk Fed Extremely Preterm Infants: A Randomized Trial

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