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Clinical Trials/NCT02027922
NCT02027922
Completed
N/A

Randomized Clinical Trial Comparing the Clinical Effectiveness of Various Professionally Applied Fluoride Prophylaxes in Deciduous Teeth in Groups at High Risk

Medical University of Warsaw0 sites180 target enrollmentNovember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
White Spot Lesion
Sponsor
Medical University of Warsaw
Enrollment
180
Primary Endpoint
the number of caries and white spot lesions in teeth treated with fluoride varnishes comparing to the control group.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The study is to compare the prophylactic and therapeutic clinical effectiveness of two fluoride varnishes in children at high caries risk.

It was hypothesized, the use of Fluor Protector S (I) fluoride varnish in children with deciduous teeth at high risk of caries (P) reduces caries and the activity/remineralisation of carious enamel spots (transformation of White Spot Lesion into D (decay)) (O), similarly to what occurs after the use of Duraphat varnish (C).

Detailed Description

The study is to compare the prophylactic and therapeutic clinical effectiveness of two fluoride varnishes in children at high caries risk. It was hypothesized, the use of Fluor Protector S (I) fluoride varnish in children with deciduous teeth at high risk of caries (P) reduces caries and the activity/remineralisation of carious enamel spots (transformation of White Spot Lesion into D (decay)) (O), similarly to what occurs after the use of Duraphat varnish (C). The question set bases on a Caries Assessment by Risk Management system basing on the occurrence of major caries causative agents (biological and medical), and also of the protective/preventive ones. Questions related to the social and economical status will be left out because of the difficulty of getting them answered honestly. Teeth will be scored according to International Caries Detection System II classification, and oral hygiene according to the Greene and Vermillion simplified Oral Hygiene Index (OHI-S) (1964). Children and their parents/guardians will receive hygienic, dietary and prophylactic guidelines.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
March 2016
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medical University of Warsaw
Responsible Party
Principal Investigator
Principal Investigator

Anna Turska Szybka

Prof Ass.

Medical University of Warsaw

Eligibility Criteria

Inclusion Criteria

  • generally healthy children aged 3-5 years
  • high risk of caries
  • parent/legal guardian consent for participation in research study

Exclusion Criteria

  • chronic diseases or medication in medical history
  • planned change of residence within a year
  • aged \<3, \>5 years

Outcomes

Primary Outcomes

the number of caries and white spot lesions in teeth treated with fluoride varnishes comparing to the control group.

Time Frame: 12 months

The primary outcome were caries prevalence and increment.The primary endpoint for each individual child is whether or not there has been any occurrence of new caries lesions over the 1 year period, as measured by any increase in d3mft at 1 years of follow up compared to the d3mft at baseline (d3mft is dental decay as measured by the dmft scale in the dentine)

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