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Does Administration of Probiotics During Infancy Increase the Caries Risk of a Child

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ClinicalTrials.gov Identifier: NCT01424852
Recruitment Status : Withdrawn (Too few of the invited subjects wanted to participate)
First Posted : August 29, 2011
Last Update Posted : February 22, 2012
Sponsor:
Information provided by (Responsible Party):
Eva Soderling, University of Turku

Brief Summary:

Aim: to examine caries occurrence in children who ten years ago received a mixture of probiotics during infancy.

Hypothesis: the administration of probiotics during infancy has no effect on future dental health.


Condition or disease Intervention/treatment Phase
Dental Caries Dietary Supplement: Probiotics in infant milk formula Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Early Administration of Bifidobacterium Lactis BB-12 and the Caries Occurence of Children a 4 Years of Age
Study Start Date : January 2012
Estimated Primary Completion Date : December 2012
Estimated Study Completion Date : December 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tooth Decay
U.S. FDA Resources

Arm Intervention/treatment
Active Comparator: Probiotics in milk formula
B. lactis BB-12 and L. rhamnosus GG delivered in milk formula during the first year of infancy
Dietary Supplement: Probiotics in infant milk formula
Probiotic infgant milk formula administered during the forst year of life
Other Name: B.lactis BB12 and L.rhamnosus GG in milk formula
Placebo Comparator: Control milk formula
The children received milk formula with no probiotics
Dietary Supplement: Probiotics in infant milk formula
Probiotic infgant milk formula administered during the forst year of life
Other Name: B.lactis BB12 and L.rhamnosus GG in milk formula



Primary Outcome Measures :
  1. Caries occurence [ Time Frame: 10 years ]

Secondary Outcome Measures :
  1. Oral microbial colonization [ Time Frame: 10 years ]


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Ages Eligible for Study:   9 Years to 12 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Child participated in the probiotic milk intervention study in early 2000
  • Child lives now within 100 km from Turku

Exclusion Criteria:

  • Child has a chronic illness affecting dental health
  • Child lives now outside 100 km from Turku

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01424852


Locations
Finland
University of Turku
Turku, Finland, 20520
Sponsors and Collaborators
University of Turku
Investigators
Study Director: Erika M Isolauri, Professor University of Turku

Responsible Party: Eva Soderling, Adjunct Professor, University of Turku
ClinicalTrials.gov Identifier: NCT01424852     History of Changes
Other Study ID Numbers: Probiotics study7.4.2011
First Posted: August 29, 2011    Key Record Dates
Last Update Posted: February 22, 2012
Last Verified: February 2012

Keywords provided by Eva Soderling, University of Turku:
Probiotics
Caries
Oral flora

Additional relevant MeSH terms:
Dental Caries
Tooth Demineralization
Tooth Diseases
Stomatognathic Diseases