A Study of a Prebiotic, a Probiotic and a Synbiotic Upon the Gut Microbiota and Immune Response of Healthy Volunteers
NCT ID: NCT01545219
Last Updated: 2012-03-07
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
44 participants
INTERVENTIONAL
2008-09-30
2010-01-31
Brief Summary
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Detailed Description
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A double-blind, placebo-controlled, randomized crossover study will be conducted in 44 healthy volunteers. The placebo will be 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 fluorescence in situ hybridisation (FISH) with 16S rRNA targeted oligonucleotide probes. Concentrations of short chain fatty acids (SCFA) will be quantified using gas chromatography (GC).
In addition to analyses performed on the samples at the University of Reading, analyses on microbial metabolites and selected members of the microbiota will also be performed at Danisco Finland, Kantvik. University of Reading will therefore provide Danisco Kantvik with faecal samples of appropriate size.
The secondary objective of this study is to examine the effects of XOS (8g/day), B. lactis BI07 (109 CFU/day) and the synbiotic (8g/day of XOS and 109 CFU/day of B. lactis BI07) on bowel function, immune function and plasma lipids in 44 healthy volunteers. This will be achieved using volunteer diaries of bowel function and mood, and by investigating total plasma lipids, mucosal immunity (salivary and faecal IgA), total leukocyte numbers, expression of cell surface markers on immune cells to identify cell subsets and activation markers, production of inflammatory markers by whole blood cultures, plasma chemokines, phagocytosis and oxidative burst by monocytes and granulocytes, plasma/serum immunoglobulins, acute phase proteins, complement proteins 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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Prebiotic
Prebiotic
8g/day xylo-oligosaccharide
Probiotic
Bi-07
10\^9 CFU B. lactis / day
Synbiotic
Synbiotic
8g/day xylo-oligosaccharide + 10\^9 CFU Bi-07
Placebo
Placebo
8g/day maltodextrin
Interventions
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Prebiotic
8g/day xylo-oligosaccharide
Bi-07
10\^9 CFU B. lactis / day
Synbiotic
8g/day xylo-oligosaccharide + 10\^9 CFU Bi-07
Placebo
8g/day maltodextrin
Eligibility Criteria
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Inclusion Criteria
* age 25-65 years
* body mass index 20-30 inclusive
* good general health as determined by medical questionnaires
Exclusion Criteria
* History of drug abuse, including alcohol
* Severe allergy or a history of severe abnormal drug reaction
* Participation in experimental drug trial within four weeks prior to study
* Participation in prebiotics or laxative trial within the previous three months
* Use of antibiotics within the previous six months
* Chronic constipation, diarrhoea or other chronic gastro-intestinal complaint
* Intake of other prebiotics or probiotics, drugs active on gastrointestinal motility, or a laxative of any class for four weeks prior to study
* Use of prescribed medication
* Regular use of aspirin or other anti-inflammatory drugs
25 Years
65 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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Glenn R Gibson, BSc, PhD
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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08/38
Identifier Type: -
Identifier Source: org_study_id
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