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LGG/BB12-pastille Study

OverviewStructured DataIssuesContributors

Contents

clinicaltrials.gov/study/NCT01577485
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT015774850
Health Conditions in Trial
Probiotics
Probiotics
0
Trial Recruitment Size
600
Trial Sponsor
University of Turku
University of Turku
0
Trial Collaborator
University of Michigan
University of Michigan
0
‌
The Forsyth Institute
0
Clinical Trial Start Date
2012
0
Primary Completion Date
2012
0
Study Completion Date
2012
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Screening0
Intervention Type
Dietary Supplement0
Interventional Trial Phase
Phase 10
Official Name
LGG/BB12-pastille Study0
Last Updated
January 4, 2013
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Quadruple0
Masked Party
Participant0
Investigator0
Care Provider0
Outcomes Assessor0

Other attributes

Intervention Treatment
Control pastille0
Probiotics in an pastille0
Study summary

We want to study the effect of short-term consumption of probiotics (a mixture of L. rhamnosus GG and B. lactis BB-12)on the composition of the oral flora.

Timeline

No Timeline data yet.

Further Resources

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Author
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Date
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References

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