The Effct of Chitooligosaccharide on Immune Function in Healthy Adults
NCT ID: NCT00468962
Last Updated: 2007-05-03
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
PHASE4
INTERVENTIONAL
Brief Summary
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This study was a 8-week, randomized, double-blind clinical trial. The 30 volunteers were divided into a control group(n=10), half dose chitooligosaccaride(FACOSTM) intake group(n=10), and full dose FACOS intake group(n=10). Peripheral blood mononuclear cells(PBMCs) were isolated and cultured in 12 well plate for 48 hours. Cytokine production by PBMCs pre- and postintervention were measured simultaneously after stimulation with lipopolysaccaride.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DOUBLE
Interventions
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FACOS (functional food)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* severe liver and kidney disease
* pregnant, lactating women
* cancer, stroke, etc.
20 Years
50 Years
ALL
No
Sponsors
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Eulji University Hospital
OTHER
Principal Investigators
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Hee-Jeong Choi, MD, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Eulji University Hospital
Other Identifiers
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07-05
Identifier Type: -
Identifier Source: org_study_id