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Prevention of Recurrent Caries With Lactobacilli PRECAL

Prevention of Recurrent Childhood Caries With Probiotic Supplement, a Randomized Controlled Trial

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04929340
Enrollment
70
Registered
2021-06-18
Start date
2017-05-01
Completion date
2021-12-01
Last updated
2021-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries in Children

Keywords

Early childhood caries, Probiotic bacteria

Brief summary

The aim of this study was to compare the effect of drops containing probiotic bacteria (Lactobacillus reuteri 17938, Lactobacillus reuteri PTA 5289, Biogaia AB, Sweden) on the incidence of dental caries with placebo drops in preschool children undergoing comprehensive restorative treatment under general anesthesia or conscious sedation. The project will be conducted at three specialist centers (Umeå University, Umeå, Sweden, Maxillo-facial unit, Halmstad Hospital, Sweden; Eastman Institute, Stockholm, Sweden) and employ a randomized placebo-controlled design with two parallel arms. The study will be performed double-blind and neither the parents nor the clinicians will be aware of the content of the drops. The follow-up period is one year.

Interventions

The children are randomly allocated to a test or a control group with aid of computer-generated numbers at the time of consent. After the treatment, children in the test group are given 5 drops per day containing probiotic bacteria (Lactobacillus reuteri Protectis DSM 17938, Biogaia AB, Sweden) before bedtime. One dose consists of a minimum of 100 million live bacteria. Children in control group are given 5 drops per day (containing no bacteria).

OTHERPlacebo

Children in control group are given 5 drops per day (containing no bacteria).

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

yellow / blue dots on the bottles indicates different groups

Eligibility

Sex/Gender
ALL
Age
2 Years to 5 Years
Healthy volunteers
No

Inclusion criteria

* Preschool children, 2-5 year of age * with Early childhood caries (ECC) or * severe Early childhood caries (S-ECC) * scheduled for restorations and extractions under general anesthesia or any form of sedation * The obligate requirement is that the child should be fully treated and managed with aspect to caries within a period of not more than two months.

Exclusion criteria

* medically comprised children * children with severe cognitive problems or dysfunctional families * families planning to relocate within the next year

Design outcomes

Primary

MeasureTime frameDescription
dental caries6 monthsdental caries (International Caries Detection and Assesment System, ICDAS level)

Secondary

MeasureTime frameDescription
visible supra-gingival plaque6 monthspresence of visible supragingival plaque on buccal surfaces upper anterior teeth (yes/no)

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026