Clinical Trials Directory

Trials / Unknown

UnknownNCT01454661

Probiotics and Early Microbial Contact in Preterm Neonates

Probiotic Modulation of Early Microbial Contact in Premature Infants

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Turku University Hospital · Other Government
Sex
All
Age
3 Days
Healthy volunteers
Accepted

Summary

Probiotics are live microbes which, when administered in sufficient amounts, confer a health benefit to the host. According to recent clinical trials, administration of probiotics to very low birth weight infants significantly reduces overall mortality and risk of necrotizing enterocolitis, a devastating inflammatory intestinal disease. The investigators have previously demonstrated that administering probiotics to the lactating mother enhances the immunoprotective properties of breast milk. Despite the promising data, the optimal probiotic intervention is yet to be established. The mechanisms by which probiotics exert their effects remain largely unknown. This research project is based on the notion that modulation of early microbial contact by probiotics may provide a safe and effective means to improve the health of preterm infants. In particular, the investigators hypothesize that the protective potential of probiotics may be enhanced via breast milk by administering probiotics to the lactating mother. All of the potentially beneficial effects of probiotic bacteria are strain-specific and therefore preliminary laboratory and clinical research with regard to different physiological targets of probiotic intervention should be carried out to guide the design of large-scale clinical trials aiming show clinical efficacy and establish clinical practice. The purpose of this research project is to identify targets for probiotic therapy in premature neonates and to provide insight into the optimal probiotic strains and administration protocol the clinical efficacy of which will subsequently be tested in a randomized controlled trial. The specific aims of the project are: 1. To determine the effect of maternal consumption of probiotics during lactation on immunomodulatory properties of breast milk in mothers of premature infants. Concentrations of immunomodulatory factors and microbiological properties of breast milk will be measured. 2. To investigate the impact of different probiotic administration protocols on gut microbiota composition in preterm infants. In particular, the issue whether maternal probiotic consumption instead or in addition to probiotics administered to the infant is effective will be elucidated. Different potential probiotic strains will be assessed. 3. To elucidate the impact probiotic bacteria administered to the lactating mother and/or directly to the infant on gut immunophysiology in preterm infants.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLGGLactobacillus rhamnosus GG 10E9 cfu / day
DIETARY_SUPPLEMENTLGG+Bb-12A combination of the probiotics Lactobacillus rhamnosus GG and Bifidobacterium lactis Bb-12 administered 10E9 cfu / day each.
DIETARY_SUPPLEMENTPlaceboMicrocrystalline cellulose is used as placebo.

Timeline

Start date
2014-04-01
Primary completion
2019-04-01
Completion
2019-04-01
First posted
2011-10-19
Last updated
2018-04-19

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01454661. Inclusion in this directory is not an endorsement.