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The Effects of Probiotic Supplementation on Extremely Low Birthweight Infants

Primary Purpose

Feeding Tolerance

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Probiotic Supplemented Group
Control Group
Sponsored by
Mercy Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Feeding Tolerance focused on measuring Probiotics, Feeding Tolerance, Extremely Low Birthweight Infants

Eligibility Criteria

undefined - 14 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Birthweight between 500-999 grams
  • Apgar score greater than or equal to 3 at 5 minutes
  • Infant free from any known major congenital anomalies or chromosomal/genetic anomalies
  • Infant without any known cyanotic or complex congenital heart disease
  • Infant NPO or on trophic enteral feedings than have been started less than 24 hours previously
  • Infant without prior history of necrotizing enterocolitis or gastrointestinal perforation
  • Infant without previous exposure to probiotics
  • Infant that will be ready to start trophic feedings within the first 14 days of life
  • Infant less than or equal to 14 days of age
  • Infant born to HIV negative mother
  • Written informed consent obtained from mother

Exclusion Criteria:

  • Infant born to HIV positive mother
  • Infant with history of prior probiotic exposure
  • Infant greater than 14 days of age
  • Infant on enteral feedings for greater than 24 hours
  • Infant with major congenital anomaly/chromosomal or genetic anomaly
  • Infant with cyanotic/complex congenital heart disease
  • Infant with previous gastrointestinal perforation/necrotizing enterocolitis
  • 5 minute Apgar score < 3

Sites / Locations

  • Rockford Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Probiotic Supplemented Group

Control Group

Arm Description

500,000,0000 cells of Lactobacillus GG (utilizing either Culturelle for Kids or Kids Culturelle preparation) and 500,000,000 cells of Bifidobacterium Infantis (utilizing Align capsule) diluted in 3 ml breastmilk/formula and administered enterally from first day of enteral feeds until term gestation/discharge/transfer/death (whichever occurs first) every day infant is receives enteral feedings

3 ml enteral feeding of breastmilk/formula administered once daily in addition to regularly prescribed enteral feedings from day of first feeding until term gestation/discharge/transfer/death (which ever occurs first) and administered every day that infant receives enteral feedings

Outcomes

Primary Outcome Measures

Feeding Tolerance
Feeding Tolerance as determined by the number of days infant is without enteral feedings due to feeding intolerance, number of days infant requires supplemental hyperalimentation/intravenous fluids for nutritional support and number of days to achieve full enteral feedings

Secondary Outcome Measures

Necrotizing Enterocolitis (Bell's Stage 2 or greater)
Culture proven sepsis without Necrotizing Enterocolitis
Chronic Lung Disease
Periventricular Leukomalacia
Mortality
Intraventricular Hemorrhage
Daily weight gain in grams
Discharge weight measured and expressed by percentile of growth for age
Length of Stay

Full Information

First Posted
February 4, 2013
Last Updated
October 9, 2018
Sponsor
Mercy Health System
Collaborators
Rockford Memorial Hospital Development Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01788761
Brief Title
The Effects of Probiotic Supplementation on Extremely Low Birthweight Infants
Official Title
The Effects of Probiotic Supplementation on Extremely Low Birthweight Infants
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Terminated
Study Start Date
July 2012 (undefined)
Primary Completion Date
July 11, 2018 (Actual)
Study Completion Date
July 11, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mercy Health System
Collaborators
Rockford Memorial Hospital Development Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a research study that will look at the effects of giving two nutritional supplements on extremely low birth infants (infants weighing less than 1000 grams or weighing less than approximately 2 lbs 3 1/2 ounces at birth). The nutritional supplements that will be studied are Culturelle for Kids/Culturelle Kids and Align. They are nutritional supplements that each contain a different probiotic. In this study the investigators will mainly be looking at the effect that these supplements may have on how well babies tolerate their feedings and how long they require supplemental intravenous fluids for nutritional support. The investigators will also, however, look at many other factors such as rate of growth, rates of infection, survival rate and the length of time the infant needs to be in the hospital. The investigators will also look at its effect on conditions/complications of prematurity such as bronchopulmonary dysplasia and chronic lung disease (chronic diseases of the lung associated with prematurity), necrotizing enterocolitis and intestinal perforations (serious diseases of the infant's intestines), retinopathy of prematurity (eye disease associated with prematurity), intracranial hemorrhage (bleeding into the brain) and patent ductus arteriosus (a blood vessel connecting two main blood vessels coming out of the heart that does not close spontaneously (by itself).
Detailed Description
The purpose of this research study is to investigate the effect of the administration of the nutritional supplements, Culturelle for Kids/Kids Culturelle in combination with Align, containing the Probiotics Lactobacillus GG and Bifidobacterium Infantis, on feeding tolerance (as determined by the number of days infant is without enteral feedings due to feeding intolerance, number of days infant requires supplemental hyperalimentation/intravenous fluids for nutritional support and number of days to achieve full enteral feedings) in high risk extremely low birth weight infants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Feeding Tolerance
Keywords
Probiotics, Feeding Tolerance, Extremely Low Birthweight Infants

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
133 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotic Supplemented Group
Arm Type
Experimental
Arm Description
500,000,0000 cells of Lactobacillus GG (utilizing either Culturelle for Kids or Kids Culturelle preparation) and 500,000,000 cells of Bifidobacterium Infantis (utilizing Align capsule) diluted in 3 ml breastmilk/formula and administered enterally from first day of enteral feeds until term gestation/discharge/transfer/death (whichever occurs first) every day infant is receives enteral feedings
Arm Title
Control Group
Arm Type
Sham Comparator
Arm Description
3 ml enteral feeding of breastmilk/formula administered once daily in addition to regularly prescribed enteral feedings from day of first feeding until term gestation/discharge/transfer/death (which ever occurs first) and administered every day that infant receives enteral feedings
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic Supplemented Group
Other Intervention Name(s)
Culture for Kids, Kids Culturelle, Align, Lactobacillus GG, Bifidobacter Infantis
Intervention Type
Dietary Supplement
Intervention Name(s)
Control Group
Other Intervention Name(s)
Breastmilk, Formula
Primary Outcome Measure Information:
Title
Feeding Tolerance
Description
Feeding Tolerance as determined by the number of days infant is without enteral feedings due to feeding intolerance, number of days infant requires supplemental hyperalimentation/intravenous fluids for nutritional support and number of days to achieve full enteral feedings
Time Frame
Evaluated on a daily basis until hospital discharge/transfer/death up until one year of age
Secondary Outcome Measure Information:
Title
Necrotizing Enterocolitis (Bell's Stage 2 or greater)
Time Frame
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until 1 year of age
Title
Culture proven sepsis without Necrotizing Enterocolitis
Time Frame
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Title
Chronic Lung Disease
Time Frame
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Title
Periventricular Leukomalacia
Time Frame
Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Title
Mortality
Time Frame
Infant's entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Title
Intraventricular Hemorrhage
Time Frame
Infants entire inpatient record assessed at/after time of hospital discharge/transfer/death up until one year of age
Title
Daily weight gain in grams
Time Frame
Measured daily until time of hospital discharge/transfer/death up until one year of age
Title
Discharge weight measured and expressed by percentile of growth for age
Time Frame
Assessed at the time of discharge/transfer/death up until one year of age
Title
Length of Stay
Time Frame
Measured at time of discharge/transfer/death up until one year of age

10. Eligibility

Sex
All
Maximum Age & Unit of Time
14 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Birthweight between 500-999 grams Apgar score greater than or equal to 3 at 5 minutes Infant free from any known major congenital anomalies or chromosomal/genetic anomalies Infant without any known cyanotic or complex congenital heart disease Infant NPO or on trophic enteral feedings than have been started less than 24 hours previously Infant without prior history of necrotizing enterocolitis or gastrointestinal perforation Infant without previous exposure to probiotics Infant that will be ready to start trophic feedings within the first 14 days of life Infant less than or equal to 14 days of age Infant born to HIV negative mother Written informed consent obtained from mother Exclusion Criteria: Infant born to HIV positive mother Infant with history of prior probiotic exposure Infant greater than 14 days of age Infant on enteral feedings for greater than 24 hours Infant with major congenital anomaly/chromosomal or genetic anomaly Infant with cyanotic/complex congenital heart disease Infant with previous gastrointestinal perforation/necrotizing enterocolitis 5 minute Apgar score < 3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kim M Schmidt, MS, APN, NNP
Organizational Affiliation
Mercy Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rockford Memorial Hospital
City
Rockford
State/Province
Illinois
ZIP/Postal Code
61103
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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The Effects of Probiotic Supplementation on Extremely Low Birthweight Infants

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