The Impact of Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Premature Infants
Primary Purpose
Fecal Microflora in the Formula Fed Premature Infant
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
ProlactPlus
GOS galacto-oligosaccharides
Bifidobacterium infantis
Bifidobacterium animalis
Sponsored by

About this trial
This is an interventional prevention trial for Fecal Microflora in the Formula Fed Premature Infant focused on measuring probiotic, prebiotic, oligosaccharides, GOS, galacto oligosaccharides, Bifidobacterium infantis, Bifidobacterium animalis
Eligibility Criteria
Inclusion Criteria:
- Born in or transferred to UCDMC within the first two weeks of life. Birth weight less than 1500 grams. Gestational age less than 33 completed weeks. Exclusively formula fed.
Exclusion Criteria:
- Gastrointestinal or cardiac anomalies.
Sites / Locations
- UC Davis Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Active Comparator
Active Comparator
Active Comparator
Arm Label
1
2
3
4
Arm Description
Permeate
GOS
Bifidobacterium infantis
Bifidobacterium animalis
Outcomes
Primary Outcome Measures
To determine the optimum dose and optimum dietary supplement to promote a fecal microflora in the formula fed premature infant that is similar to that of the term breast fed infant (a predominance of bifidobacteria).
Secondary Outcome Measures
Full Information
NCT ID
NCT00810160
First Posted
December 15, 2008
Last Updated
July 11, 2017
Sponsor
University of California, Davis
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
1. Study Identification
Unique Protocol Identification Number
NCT00810160
Brief Title
The Impact of Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Premature Infants
Official Title
Phase 1A Study of Impact of Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Premature Infants
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to see whether dietary supplements can change the germs in the intestines of premature infants to be more like those of healthy breast fed term babies.
Detailed Description
To determine the optimum dose and optimum dietary supplement to promote a fecal microflora in the formula fed premature infant that is similar to that of the term breast fed infant (a predominance of bifidobacteria). In the initial phase of this trial, 30 premature infants will be randomly assigned to receive increasing doses of one of four dietary supplements: Permeate (a pasteurized human milk concentrate containing human milk oligosaccharides processed by Prolacta), GOS (galacto-oligosaccharides manufactured by Friesland foods), Bifidobacterium infantis or Bifidobacterium animalis. Weekly stool specimens will be examined by PCR to determine content of bifidobacteria and total bacteria. This study is limited to formula fed infants in order to avoid the confounding effects of the human milk oligosaccharides in breast milk. An additional 12 human milk fed infants will be enrolled and will have their diet supplemented with ProlactPlus (a pasteurized human milk concentrate containing humna milk oligosaccharides) or powdered human milk fortifier for comparison
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Microflora in the Formula Fed Premature Infant
Keywords
probiotic, prebiotic, oligosaccharides, GOS, galacto oligosaccharides, Bifidobacterium infantis, Bifidobacterium animalis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
59 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Permeate
Arm Title
2
Arm Type
Active Comparator
Arm Description
GOS
Arm Title
3
Arm Type
Active Comparator
Arm Description
Bifidobacterium infantis
Arm Title
4
Arm Type
Active Comparator
Arm Description
Bifidobacterium animalis
Intervention Type
Dietary Supplement
Intervention Name(s)
ProlactPlus
Other Intervention Name(s)
human milk oligosaccharides
Intervention Description
Group 1 infants will be fed a concentration of Permeate mixed with formula. The ProlactPlus will be increased each week as follows: week 1 95:5 (formula:ProlactPlus), week 2 90:10, week 3 85:15, week 4 80:20, and week 5 75:25. Caloric content is roughly as follows: week 1 21 cal/oz, week 2 22 cal/oz, week 3 23 cal/oz, week 4 24 cal/oz, and week 5 25 cal/oz.
Intervention Type
Dietary Supplement
Intervention Name(s)
GOS galacto-oligosaccharides
Other Intervention Name(s)
galacto-oligosaccharides
Intervention Description
Group 2 infants will have their formula supplemented with galacto-oligosaccharides (GOS) for each feeding as follows: week 1 0.25 g/dL, week 2 0.5 g/dL, week 3 1.0 g/dL, week 4 1.5 g/dL, and week 5 2.0 g/dL.
Intervention Type
Dietary Supplement
Intervention Name(s)
Bifidobacterium infantis
Other Intervention Name(s)
bifidobacteria, B. infantis
Intervention Description
Group 3 infants will have their formula supplemented with B. infantis twice daily increasing the dose each week as follows: week 1 5x107, week 2 1.5x108, week 3 4.5x108, week 4 1.4x109, and week 5 4.2x109.
Intervention Type
Dietary Supplement
Intervention Name(s)
Bifidobacterium animalis
Other Intervention Name(s)
B. animalis, bifidobacteria
Intervention Description
Group 4 infants will have their formula supplemented with B. animalis twice daily increasing the dose each week as follows: week 1 5x107, week 2 1.5x108, week 3 4.5x108, week 4 1.4x109, and week 5 4.2x109.
Primary Outcome Measure Information:
Title
To determine the optimum dose and optimum dietary supplement to promote a fecal microflora in the formula fed premature infant that is similar to that of the term breast fed infant (a predominance of bifidobacteria).
Time Frame
six weeks
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Born in or transferred to UCDMC within the first two weeks of life. Birth weight less than 1500 grams. Gestational age less than 33 completed weeks. Exclusively formula fed.
Exclusion Criteria:
Gastrointestinal or cardiac anomalies.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Underwood, MD
Organizational Affiliation
University of California, Davis
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Davis Medical Center
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
23993139
Citation
Underwood MA, Kalanetra KM, Bokulich NA, Lewis ZT, Mirmiran M, Tancredi DJ, Mills DA. A comparison of two probiotic strains of bifidobacteria in premature infants. J Pediatr. 2013 Dec;163(6):1585-1591.e9. doi: 10.1016/j.jpeds.2013.07.017. Epub 2013 Aug 29.
Results Reference
derived
Learn more about this trial
The Impact of Oligosaccharides and Bifidobacteria on the Intestinal Microflora of Premature Infants
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