LGG/BB12-pastille Study

Phase 1

Completed

• Conditions: Probiotics
• Interventions: Dietary Supplement: Probiotics in an pastille; Dietary Supplement: Control pastille

• Registration Number: NCT01577485
• Lead Sponsor: University of Turku

Brief 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2012-04-12
• Study First Submitted QC: 2012-04-12
• Study First Posted: 2012-04-13
• Study Start: 2012-08
• Primary Completion: 2012-11
• Study Completion: 2012-11
• Status Verified: 2013-01
• Last Update Submitted: 2013-01-03
• Last Update Posted: 2013-01-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Subjects healthy, 20-30 yrs of age

Exclusion Criteria

• Subjects not healthy, too old/young

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Probiotic pastille	Probiotics in an pastille	Test group
Control pastille	Control pastille	Control group

Primary Outcome Measures

Name	Time	Method
Counts of mutans streptococci	4 weeks

Secondary Outcome Measures

Name	Time	Method
Amount of plaque	4 weeks

Trial Locations

Locations (1)

Institute of Dentistry; 🇫🇮 Turku, Finland