Evaluation of Safety, Tolerance and Effects on the Intestinal Flora of a New Fermented Milk for Preterm Infants
Primary Purpose
Preterms With Gestational Age Ranging From 30 to 35 Weeks
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Milk with probiotic and prebiotic activities
Milk without probiotic and prebiotic activities
Sponsored by

About this trial
This is an interventional prevention trial for Preterms With Gestational Age Ranging From 30 to 35 Weeks focused on measuring Premature birth,, infant,, infant formula,, bacterial colonization,, Bifidobacterium,, calprotectin
Eligibility Criteria
Inclusion Criteria:
- Preterms with gestational age ranging from 30 to 35 weeks
- Eutrophic
- Formula feeding
Exclusion Criteria:
- Malformation or metabolic disease
- Newborns whose parents did not provide informed consent
- Contraindication to enteral feeding
Sites / Locations
- Neonatat unit, Saint Vincent de Paul Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
1
2
Arm Description
the fermented preterm formula (FPF)
formula adapted for preterm infants (PF)
Outcomes
Primary Outcome Measures
Follow-up of the number of colonized infants and the bacterial colonization levels
Secondary Outcome Measures
Clinical tolerance
Levels of intestinal immune and inflammatory markers
Full Information
NCT ID
NCT00711633
First Posted
July 4, 2008
Last Updated
July 4, 2008
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Blédina SA, Villefranche sur Saône, France
1. Study Identification
Unique Protocol Identification Number
NCT00711633
Brief Title
Evaluation of Safety, Tolerance and Effects on the Intestinal Flora of a New Fermented Milk for Preterm Infants
Official Title
Evaluation of a Fermented Formula Without Live Bacteria for Preterm Infants: Effects on Microbiota Species and Intestinal Inflammatory Markers
Study Type
Interventional
2. Study Status
Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
December 2002 (undefined)
Primary Completion Date
February 2005 (Actual)
Study Completion Date
June 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Blédina SA, Villefranche sur Saône, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The intestinal flora is a complex ecosystem which is known to play various important functions in the gut. Recent data have reported a delay in intestinal colonization in preterm. Modulating the intestinal flora through dietary supplementation with probiotics or prebiotics has been shown to improve digestive and general outcomes in full-term infants.The aim of this study was to evaluate the clinical tolerance, the effect on gut microbiota, and the mucosal inflammatory responses to a fermented milk in preterm infants.
Detailed Description
This prospective, randomized, double-blind, controlled study evaluated the safety and effect on gut microbiota, and the mucosal inflammatory responses to a fermented milk in preterm infants. Preterm infants with a gestational age (GA) ranging from 30 to 35 weeks and whose mother chose formula feeding were enrolled during their first three days of life. Both parents provided informed written consent. Infants were randomly assigned to receive either the fermented preterm formula (FPF) or, as a control, a formula adapted for preterm infants (PF). The PF was formulated to meet the nutritional needs of preterm infants. The FPF was identical, except for a manufacturing process including a fermentation step with two probiotic strains, Bifidobacterium breve C50 and Streptococcus thermophilus 065, inactivated by heat at the end of the manufacturing process. This process conferred a probiotic/prebiotic activity.For each neonate, background information about the pregnancy and neonatal parameters were collected. Anthropometric parameters (weight, height, head circumference); gastrointestinal tolerance parameters (abdominal distension, gastric residuals, rectal bleeding, NEC); drug administration; and intake of formula and mother's milk were recorded twice a week until discharge. Stools were collected twice a week from diapers for microbiological analysis and measurement of fecal inflammatory markers. All samples were immediately stored at -80°C.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterms With Gestational Age Ranging From 30 to 35 Weeks
Keywords
Premature birth,, infant,, infant formula,, bacterial colonization,, Bifidobacterium,, calprotectin
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
58 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
the fermented preterm formula (FPF)
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
formula adapted for preterm infants (PF)
Intervention Type
Dietary Supplement
Intervention Name(s)
Milk with probiotic and prebiotic activities
Intervention Description
Comparison of two different formula for preterm infants
Intervention Type
Dietary Supplement
Intervention Name(s)
Milk without probiotic and prebiotic activities
Other Intervention Name(s)
Comparison of formula for preterm infants
Intervention Description
Comparison of formula for preterm infants
Primary Outcome Measure Information:
Title
Follow-up of the number of colonized infants and the bacterial colonization levels
Time Frame
weekly until hospital discharge
Secondary Outcome Measure Information:
Title
Clinical tolerance
Time Frame
weekly until hospital discharge
Title
Levels of intestinal immune and inflammatory markers
Time Frame
weekly until hospital discharge
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
15 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Preterms with gestational age ranging from 30 to 35 weeks
Eutrophic
Formula feeding
Exclusion Criteria:
Malformation or metabolic disease
Newborns whose parents did not provide informed consent
Contraindication to enteral feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Florence Campeotto, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neonatat unit, Saint Vincent de Paul Hospital
City
Paris
ZIP/Postal Code
75014
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
17541346
Citation
Campeotto F, Waligora-Dupriet AJ, Doucet-Populaire F, Kalach N, Dupont C, Butel MJ. [Establishment of the intestinal microflora in neonates]. Gastroenterol Clin Biol. 2007 May;31(5):533-42. doi: 10.1016/s0399-8320(07)89424-3. French.
Results Reference
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Evaluation of Safety, Tolerance and Effects on the Intestinal Flora of a New Fermented Milk for Preterm Infants
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