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Completed

NCT Number: NCT01577485

LGG/BB12-pastille Study

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.

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Key information

Conditions

Probiotics

Age range

20 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Institute of Dentistry

Turku, 20520, Finland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects healthy, 20-30 yrs of age

Exclusion criteria

  • Subjects not healthy, too old/young

Treatment and study plan

Probiotics in an pastille

Dietary Supplement

Test group

Control pastille

Dietary Supplement

Control group

Primary outcomes

  1. Counts of mutans streptococci

    Time frame: 4 weeks

Secondary outcomes

  1. Amount of plaque

    Time frame: 4 weeks

Sponsors and collaborators

Lead sponsor

University of Turku

Other

Collaborators

  • The Forsyth Institute
  • University of Michigan

Registry information

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Apr 13, 2012
Registry last updated
Jan 4, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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