LGG/BB12-pastille Study

University of Turku

Status and phase: Completed; Phase 1

Conditions: Probiotics

Treatments: Dietary Supplement: Probiotics in an pastille; Dietary Supplement: Control pastille

Study type: Interventional

Funder types: Other

Identifiers

NCT01577485

ETMK:22/180/2012

Details and patient eligibility

About

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.

Enrollment: 60 patients

Sex: All

Ages: 20 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subjects healthy, 20-30 yrs of age

Exclusion criteria

• Subjects not healthy, too old/young

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 2 patient groups

Probiotic pastille

Experimental group

Description:

Test group

Treatment:

Dietary Supplement: Probiotics in an pastille

Control pastille

Active Comparator group

Description:

Control group

Treatment:

Dietary Supplement: Control pastille