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Human Milk for Congenital Gastrointestinal Disorders (HM for CGD)

Primary Purpose

Congenital Gastrointestinal Disorders

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Human Milk
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Congenital Gastrointestinal Disorders focused on measuring Digestive Disease and Disorders, Neonatal, Pediatric Disorders

Eligibility Criteria

1 Minute - 1 Year (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Admission to participating NICU at less than 7 days of age
  2. Birthweight >1250g and/or gestational age at birth >32 weeks
  3. Less than 7 days of enteral feedings
  4. Diagnosis of eligible primary "Congenital Gastointestinal Disorders" defined as: gastroschisis, omphalocele and intestinal atresias
  5. Consent to the use of donor human milk products
  6. Consent to participate in this study

Exclusion Criteria:

  1. Admission to participating NICU at >7 days of age
  2. Birthweight <1250g and/or gestational age <32 weeks
  3. Diagnosis of non-eligible gastrointestinal disorders: congenital diaphragmatic hernia, midgut volvulus, Hirschsprung's disease, esophageal atresia, imperforate anus
  4. Evidence of significant liver dysfunction at time of enrollment (direct bilirubin >4 and transaminases elevated more than 2 SD above upper limit of normal for age)
  5. Liver malformations such as biliary atresia and choledochal cyst
  6. Refusal of consent

Sites / Locations

  • Children's Healthcare of Atlanta-Egleston

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Retrospective Control Group

Exclusive Human Milk Diet Group

Arm Description

Approximately 150 patients with congenital gastrointestinal disorders who were treated in the neonatal intensive care unit (NICU) at Children's Healthcare of Atlanta-Egleston and other participating institutions from 2012 to 2015, who had non-human milk (HM) diets will be identified as retrospective controls using the electronic medical records system.

A minimum of 150 patients with CGD admitted to participating NICUs who meet inclusion criteria and provide informed consent will be enrolled in the prospective arm of the study. These patients will be fed an EHMD comprised of mother's own milk (MOM) or pasteurized donor human milk (DM). Fortification will be provided with human milk derived human milk fortifier, either a human milk-based fortifier (Prolact+ H2MF®) for infants born at less than 37 weeks GA or <2,200g birth weight or the term-equivalent version (PBCLN-002) formulated for infants >37 weeks and/or >2,200g at birth. Infants will receive this EHMD until they have achieved full enteral feedings for 7 days with bowel in continuity

Outcomes

Primary Outcome Measures

Time to full enteral feeding
The number of days to achieve full enteral feeding after the initial human milk feeding

Secondary Outcome Measures

Number of days of parenteral nutrition
The total number of days parenteral nutrition is required.
Growth
Compare growth parameters (weight, length and head circumference) as daily g/kg/d and z-scores birth to discharge
Difference in conjugated bilirubin levels
The difference in average bilirubin level will be compared between the non-human milk diet (retrospective control group) and the breast milk diet group.
Length of hospital stay
The length of hospital stay described as the number of days spent in the hospital
Feeding interruptions
NPO for at least 24 hours. NPO due to elective surgeries or procedures will not be defined as feeding interruptions
Feeding intolerance
Number of days when one or more feedings were held for clinical concerns
Episodes of Necrotizing Enterocolitis
Number of episodes of Stage IIb NEC or greater
Number of sepsis episodes
The number of sepsis episodes will be compared between the non-breast milk diet (retrospective control group) and the breast milk diet group.
Death rate
The number of deaths between participants who receive breast milk only diets as compared to the non-breast milk diet (retrospective control group while in the neonatal intensive care unit (NICU).

Full Information

First Posted
October 1, 2015
Last Updated
August 25, 2023
Sponsor
Emory University
Collaborators
Chatham Valley Foundation, Prolacta Bioscience
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1. Study Identification

Unique Protocol Identification Number
NCT02567292
Brief Title
Human Milk for Congenital Gastrointestinal Disorders
Acronym
HM for CGD
Official Title
Effects of an Exclusive Human Milk Diet on Enteral Feeding Outcomes of Neonates With Congenital Gastrointestinal Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
July 26, 2018 (Actual)
Primary Completion Date
January 18, 2022 (Actual)
Study Completion Date
January 18, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Chatham Valley Foundation, Prolacta Bioscience

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to identify whether an exclusive human milk diet (EHMD) would improve outcomes in neonates with congenital gastrointestinal disorders (CGD) and by facilitating an earlier transition off of parenteral nutrition (PN).
Detailed Description
Infants born with congenital gastrointestinal disorders (CGD) can be very challenging to treat. The CGD require surgery shortly after birth to correct the problems and recovery can take a long time. During the period of time the infant's intestines are sick or don't work properly, they rely on parenteral nutrition (IV fluids containing carbohydrates, proteins and fats) to meet their nutritional needs. Being on PN for a long time requires special intravenous lines, and increases the risk of blood stream infections and can make the liver sick. Feeding babies who have these CGD is often very difficult, as the intestine needs to adapt. It needs to make appropriately formed stool to eliminate wastes, but not lose too much water or too many electrolytes. There is often a lot of starting and stopping of feeds. Human milk (HM) is considered the ideal source of nutrition for all infants. This study aims to identify whether an exclusive human milk diet (EHMD) would improve outcomes in neonates with congenital gastrointestinal disorders (CGD) and by facilitating an earlier transition off of parenteral nutrition (PN).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Gastrointestinal Disorders
Keywords
Digestive Disease and Disorders, Neonatal, Pediatric Disorders

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
151 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Retrospective Control Group
Arm Type
No Intervention
Arm Description
Approximately 150 patients with congenital gastrointestinal disorders who were treated in the neonatal intensive care unit (NICU) at Children's Healthcare of Atlanta-Egleston and other participating institutions from 2012 to 2015, who had non-human milk (HM) diets will be identified as retrospective controls using the electronic medical records system.
Arm Title
Exclusive Human Milk Diet Group
Arm Type
Experimental
Arm Description
A minimum of 150 patients with CGD admitted to participating NICUs who meet inclusion criteria and provide informed consent will be enrolled in the prospective arm of the study. These patients will be fed an EHMD comprised of mother's own milk (MOM) or pasteurized donor human milk (DM). Fortification will be provided with human milk derived human milk fortifier, either a human milk-based fortifier (Prolact+ H2MF®) for infants born at less than 37 weeks GA or <2,200g birth weight or the term-equivalent version (PBCLN-002) formulated for infants >37 weeks and/or >2,200g at birth. Infants will receive this EHMD until they have achieved full enteral feedings for 7 days with bowel in continuity
Intervention Type
Other
Intervention Name(s)
Human Milk
Intervention Description
Participants will receive an exclusive human milk diet comprised of mother's own milk (MOM, pasteurized donor human milk (DM) fortified with a donor-milk based fortifier (DMBF): Prolact+ for infants <37 weeks PMA and/or or weight <2,200g or PBCLN-002 for infants >37 weeks PMA and/or weight >2,200g)
Primary Outcome Measure Information:
Title
Time to full enteral feeding
Description
The number of days to achieve full enteral feeding after the initial human milk feeding
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Secondary Outcome Measure Information:
Title
Number of days of parenteral nutrition
Description
The total number of days parenteral nutrition is required.
Time Frame
Through study completion, up to 1 year
Title
Growth
Description
Compare growth parameters (weight, length and head circumference) as daily g/kg/d and z-scores birth to discharge
Time Frame
Through study completion, up to 1 year
Title
Difference in conjugated bilirubin levels
Description
The difference in average bilirubin level will be compared between the non-human milk diet (retrospective control group) and the breast milk diet group.
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Title
Length of hospital stay
Description
The length of hospital stay described as the number of days spent in the hospital
Time Frame
Through study completion, up to 6 months
Title
Feeding interruptions
Description
NPO for at least 24 hours. NPO due to elective surgeries or procedures will not be defined as feeding interruptions
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Title
Feeding intolerance
Description
Number of days when one or more feedings were held for clinical concerns
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Title
Episodes of Necrotizing Enterocolitis
Description
Number of episodes of Stage IIb NEC or greater
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Title
Number of sepsis episodes
Description
The number of sepsis episodes will be compared between the non-breast milk diet (retrospective control group) and the breast milk diet group.
Time Frame
From birth to day of life full enteral feedings for 7 days is achieved (up to 30 days)
Title
Death rate
Description
The number of deaths between participants who receive breast milk only diets as compared to the non-breast milk diet (retrospective control group while in the neonatal intensive care unit (NICU).
Time Frame
Through study completion, up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admission to participating NICU at less than 7 days of age Birthweight >1250g and/or gestational age at birth >32 weeks Less than 7 days of enteral feedings Diagnosis of eligible primary "Congenital Gastointestinal Disorders" defined as: gastroschisis, omphalocele and intestinal atresias Consent to the use of donor human milk products Consent to participate in this study Exclusion Criteria: Admission to participating NICU at >7 days of age Birthweight <1250g and/or gestational age <32 weeks Diagnosis of non-eligible gastrointestinal disorders: congenital diaphragmatic hernia, midgut volvulus, Hirschsprung's disease, esophageal atresia, imperforate anus Evidence of significant liver dysfunction at time of enrollment (direct bilirubin >4 and transaminases elevated more than 2 SD above upper limit of normal for age) Liver malformations such as biliary atresia and choledochal cyst Refusal of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heidi Karpen, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare of Atlanta-Egleston
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27331420
Citation
Shinnick JK, Wang E, Hulbert C, McCracken C, Sarson GY, Piazza A, Karpen H, Durham MM. Effects of a Breast Milk Diet on Enteral Feeding Outcomes of Neonates with Gastrointestinal Disorders. Breastfeed Med. 2016 Aug;11(6):286-292. doi: 10.1089/bfm.2016.0002. Epub 2016 Jun 22.
Results Reference
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Human Milk for Congenital Gastrointestinal Disorders

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