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Completed

NCT Number: NCT00711633

Evaluation of Safety, Tolerance and Effects on the Intestinal Flora of a New Fermented Milk for Preterm Infants

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.

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Key information

Age range

1 day–15 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Neonatat unit, Saint Vincent de Paul Hospital

Paris, 75014, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Milk with probiotic and prebiotic activities

Dietary Supplement

Comparison of two different formula for preterm infants

Milk without probiotic and prebiotic activities

Dietary Supplement

Comparison of formula for preterm infants

Other names: Comparison of formula for preterm infants

Primary outcomes

  1. Follow-up of the number of colonized infants and the bacterial colonization levels

    Time frame: weekly until hospital discharge

Secondary outcomes

  1. Clinical tolerance

    Time frame: weekly until hospital discharge

  2. Levels of intestinal immune and inflammatory markers

    Time frame: weekly until hospital discharge

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • Blédina SA, Villefranche sur Saône, France

Registry information

Official study title

Evaluation of a Fermented Formula Without Live Bacteria for Preterm Infants: Effects on Microbiota Species and Intestinal Inflammatory Markers

Important dates

Study start
2002
Primary completion
2005
Study completion
2007
First posted
Jul 9, 2008
Registry last updated
Jul 9, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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