Effect of the Amount of Fluoride Toothpaste on Fluoride Availability in the Oral Fluids in Children

NCT ID: NCT03455621

Last Updated: 2018-03-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-03-01

Study Completion Date

2011-06-30

Brief Summary

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The aim of the study is to determine the fluoride availability in saliva and dental biofilm after the use of increasing amounts of fluoride toothpaste. Using a crossover and blind design, 15 children (18-42 months old) had their teeth brushed with increasing amounts of fluoride toothpaste. Fluoride concentration in saliva and dental biofilm was determined up to 30 min after brushing.

Detailed Description

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The aim of the study is to determine the fluoride availability in saliva and dental biofilm after the use of increasing amounts of fluoride toothpaste. Children from 18 to 42 months from a community daycare participated. The study had a crossover and blind design. The amounts of toothpastes tested were: 1. A pea-size amount (0.3 g) of a non-F toothpaste; 2. 0.025 g of a F toothpaste (1,100 ppm F, as NaF); 3. 0.05 g of the same F toothpaste; 4. 0.1 g of the same F toothpaste; or 5. 0.3 g (pea-size) of the same F toothpaste. Children were to brush their teeth with the designated amount of toothpaste twice/day from Monday to Friday. In order to allow biofilm accumulation, caregivers were instructed to brush only the occlusal surfaces of primary molars. On Friday morning, at least one hour after breakfast, saliva and one biofilm sample from the right or left hemiarch were collected and analyzed for fluoride concentration. Then, brushing with the respective amount of toothpaste was performed, and saliva was collected 5, 15 and 30 min later. The biofilm from the other side of the mouth was collected after 30 min. Fluoride concentration in saliva and biofilm samples was determined with an ion-specific electrode.

Conditions

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Dental Caries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Pea-size amount of non-F dentifrice

Non-fluoride dentifrice (0 ppm F); to be used twice/day. Amount to be used: 0.3 g (pea-size amount)

Group Type PLACEBO_COMPARATOR

Toothbrushing

Intervention Type PROCEDURE

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

0.025 g of 1,100 ppm F dentifrice

Fluoride dentifrice (1,100 ppm F, as NaF); to be used twice/day. Amount to be used: 0.025 g

Group Type EXPERIMENTAL

Toothbrushing

Intervention Type PROCEDURE

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

0.05 g of 1,100 ppm F dentifrice

Fluoride dentifrice (1,100 ppm F, as NaF); to be used twice/day. Amount to be used: 0.05 g

Group Type EXPERIMENTAL

Toothbrushing

Intervention Type PROCEDURE

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

0.1 g of 1,100 ppm F dentifrice

Fluoride dentifrice (1,100 ppm F, as NaF); to be used twice/day. Amount to be used: 0.1 g

Group Type EXPERIMENTAL

Toothbrushing

Intervention Type PROCEDURE

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

Pea-size amount of 1,100 ppm F dentifrice

Fluoride dentifrice (1,100 ppm F, as NaF); to be used twice/day. Amount to be used: 0.3 g (pea-size amount)

Group Type ACTIVE_COMPARATOR

Toothbrushing

Intervention Type PROCEDURE

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

Interventions

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Toothbrushing

Toothbrushing with different amounts of fluoride toothpaste (or a non-fluoride toothpaste as a control)

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All children with an informed consent signed by the parents/guardians

Exclusion Criteria

* Children with at least on active caries lesion
Minimum Eligible Age

18 Months

Maximum Eligible Age

42 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Campinas, Brazil

OTHER

Sponsor Role lead

Responsible Party

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Livia Maria Andaló Tenuta

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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FOPBioq007

Identifier Type: -

Identifier Source: org_study_id

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