The Effect of a Prebiotic, Probiotic and Synbiotic on the Gut Microbiota and Immune Response of Older Volunteers (GOS)
NCT ID: NCT01586247
Last Updated: 2012-04-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2008-03-31
2009-10-31
Brief Summary
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Detailed Description
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A double-blind, placebo-controlled, randomized crossover study will be conducted in 40 healthy older (≥60 years of age) volunteers. The placebo will consist of maltodextrin (a food grade ingredient, administered at 8g/day).
Changes in the gut microbiota will be determined by measuring bacterial population levels in human faeces using 16S rRNA targeted oligonucleotide probes and fluorescence in situ hybridisation. Faecal pH will be measured and the production of short chain fatty acids (SCFA) will be analysed and quantified using high performance liquid chromatography (HPLC).
The secondary objective of this study is to examine the effect on cellular immune function. This will be achieved by investigating phagocytosis activity, natural killer cells which are CD4+, CD8+, CD25+ and CD2+ and CD3+ subsets, the marker of T-cell maturation period., salivary IgA levels, inflammatory markers (plasma - tumour necrosis factor (TNF), IL6, IL1, chemokines and soluble adhesion molecules).
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
TRIPLE
Study Groups
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Synbiotic
8g/day gluco-oligosaccharide + 109 CFU/day B. lactis BI07
Synbiotic
8g/day galacto-oligosaccharide + 10\^9 CFU/day B.lactis
Placebo
8g/day maltodextrin
Placebo
8g/day maltodextrin
Prebiotic
8g/day galacto-oligosaccharides (GOS)
Prebiotic
8g/day galacto-oligosaccharide
Probiotic
109 CFU/day B. lactis BI07
Probiotic
10\^9 CFU/day B.lactis
Interventions
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Synbiotic
8g/day galacto-oligosaccharide + 10\^9 CFU/day B.lactis
Placebo
8g/day maltodextrin
Prebiotic
8g/day galacto-oligosaccharide
Probiotic
10\^9 CFU/day B.lactis
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* age \>60 years
* good general health
* not in the residential care.
Exclusion Criteria
* planned major surgery
* use of antibiotics within the previous six months
60 Years
ALL
Yes
Sponsors
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Danisco
INDUSTRY
University of Reading
OTHER
Responsible Party
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Caroline Childs
Post doctoral research fellow
Principal Investigators
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Robert A Rastall
Role: PRINCIPAL_INVESTIGATOR
University of Reading
Locations
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University of Reading
Reading, Berkshire, United Kingdom
Countries
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Other Identifiers
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07/47
Identifier Type: -
Identifier Source: org_study_id
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