Dental Fluorosis Risk by the Use of Acidulated Fluoride Dentifrice

Sponsor
Federal University of Paraíba (Other)
Overall Status
Completed
CT.gov ID
NCT03761485
Collaborator
(none)
452
3
36

Study Details

Study Description

Brief Summary

This research aimed to evaluate the risk of dental fluorosis by using an experimental fluoridated acidulated dentifrice compared to conventional dentifrices in two-to-four-year-old children residing in a non fluoridated area by the concentration of fluoride incorporated in childrens' nails, as well as the incorporation of F into the biofilm. Two hundred and ten children participated on this study. They were randomly allocated into three groups differing according to the type of dentifrice used over 12 months: G1:1100 ppm F, pH 4.5; G2:750 ppm F, pH 4.5; G3:1100 ppm F, pH 7.0. The dentifrice was placed on the toothbrush using the "drop" technique. The toenails of the biggest toe were collected in three moments, corresponding to the experimental period of use of the dentifrices (T1, T2 and T3), as well as the biofilm which was collected twice, 5 and 60 minutes after brushing. The nails and biofilm fluoride concentration were analyzed on a specific electrode using the HMDS diffusion facilitated technique.

Condition or Disease Intervention/Treatment Phase
  • Other: Use of Dentifrice Fluoride
Phase 4

Detailed Description

This is a randomized, double-blind, interventional trial, adopting a strategy for collecting data, collecting data from the children's biofilm. This study was carried out in three Child Education Reference Centers (CREIs) located in different points of the city of João Pessoa PB.

The city is located in the Northeast region of Brazil, on the coast of the state of Paraíba and has about 600 thousand inhabitants (IBGE, 2013). João Pessoa has already had fluoridated water for a period of two years until the mid-1980s, but so far the project has been deactivated.

The 452 children participating in the study were divided into three groups according to the dentifrice used in a 12 - month period: G1: 1,100 ppm F - pH 4.5; G2: 750 ppm F-pH 4.5; and G3: 1100 ppm F-pH 7.0. The toothpaste was supplied by Oralls (São Jose dos Campos-SP, Brazil) and dental brushes by Bitufo (Hypermarcas, São Paulo, SP-, Brazil) and there was no conflict of interest. For the random distribution of the groups, the CREIs were considered as units, so that only one type of toothpaste was distributed in each CREI, thus facilitating the control of the dentifrices delivery by the teachers, as well as the supervised brushing in CREI itself.

The toenails of the biggest toe were collected in three moments, corresponding to the experimental period of use of the dentifrices (T1, T2 and T3), as well as the biofilm which was collected twice, 5 and 60 minutes after brushing. The nails and biofilm fluoride concentration were analyzed on a specific electrode using the HMDS diffusion facilitated technique.

Nails of the large toes were collected because they provide a sufficient nail mass for analysis and because there has been a reported possibility of contamination of the toenails (Buzalaf, Pessan et al., 2006). The nail samples of each child were cleaned with deionized water using a dental brush, taken to the ultrasound apparatus with deionized water for 10 min, dried at 60 ± 5 ° C and weighed on the analytical balance The presence of F was analyzed as described in the previous item, according to the method of Taves (1968), as modified by Whitford (1996). F patterns (0.00475, 0.0095, 0.019, 0.095, 0.190 and 0.95 mg F) were prepared by serial dilution of a stock solution of 0.1 MF (Orion) in triplicate and diffused in the same manner as the samples. The average repeatability of the readings based on duplicate samples was 95%. Whenever the sample weight was> 20 mg, the analysis was performed in duplicate.

Study Design

Study Type:
Interventional
Actual Enrollment :
452 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized double blind clinical trialRandomized double blind clinical trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
double blind
Primary Purpose:
Treatment
Official Title:
Dental Fluorosis Risk by the Use of Acidulated Fluoride Dentifrice: Clinical Trial - Epidemiological Study With Children Residing in an área Without Public Water Fluoridation
Actual Study Start Date :
Jan 15, 2015
Actual Primary Completion Date :
Jan 15, 2018
Actual Study Completion Date :
Jan 15, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dentifrice 750 ppm of NaF acidulated

Use of Dentifrice Fluoride Use of few of dentifrice on brushing for 12 months

Other: Use of Dentifrice Fluoride
Use of few of dentifrice on brushing during a year

Active Comparator: Dentifrice 1.100 ppm of NaF neutral

Use of Dentifrice Fluoride Use of few of dentifrice on brushing for 12 months

Other: Use of Dentifrice Fluoride
Use of few of dentifrice on brushing during a year

Active Comparator: Dentifrice 1.100 ppm of NaF acidulated

Use of Dentifrice Fluoride Use of few of dentifrice on brushing for 12 months

Other: Use of Dentifrice Fluoride
Use of few of dentifrice on brushing during a year

Outcome Measures

Primary Outcome Measures

  1. Concentration of intraoral fluoride [1 year]

    Effective of capacity to concentration of fluoride in biofilm (ppm)

  2. Effect of intraoral fluoride - software [1 year]

    Reduction of initial lesions carie give by mm² analysed by software

  3. Effect of intraoral fluoride [1 year]

    Reduction of initial lesions carie give by visual scale (Nyvad scale)

  4. Concentration of nail fluorid [1 year]

    Concentration of fluoride in nail (ppm)

Eligibility Criteria

Criteria

Ages Eligible for Study:
2 Years to 4 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age group of 2 to 4 years of age of both sexes

  • Who were enrolled in one of the 3 CREIs that participated in the research

  • Presence of deciduos teeth

Exclusion Criteria:
  • Presented high mobility of the children (incompatible with the planning of a longitudinal study)

  • Children who did not allow the clinical examination in the school

  • Children using orthodontic appliances or children with extensive caries lesions with dentin sensitivity

  • Children not residing in the city of João Pessoa-PB from birth to 4 years due to the fluoridation of water from public supply.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Federal University of Paraíba

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fabio Correia Sampaio, Professor, Federal University of Paraíba
ClinicalTrials.gov Identifier:
NCT03761485
Other Study ID Numbers:
  • Acidulated fluoride dentifrice
First Posted:
Dec 3, 2018
Last Update Posted:
Dec 3, 2018
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 3, 2018