Effectiveness of Sealants on Molars (sealants)

University Hospital Center (CHU)

Status: Completed

Conditions: Tooth Decay

Treatments: Other: decayed tooth surfaces

Study type: Interventional

Funder types: Other

Identifiers

NCT02896088

9500

Details and patient eligibility

About

Currently, the real scope of sealants (AS) is poorly documented in temporary dentition and its effectiveness has not been demonstrated. Yet it seems reasonable that the AS in temporary dentition could slow the specific development of carious lesions in early childhood. In addition, this non-invasive approach could delay the conventional food and thus save financial costs for more complex treatments. Finally, the installation of AS could afford, as demonstrated in adult teeth, lowering the cariogenic bacteria prevalence engaged in the caries process.

Full description

Currently, the real scope of sealants (AS) is poorly documented in temporary dentition and its effectiveness has not been demonstrated. Yet it seems reasonable that the AS in temporary dentition could slow the specific development of carious lesions in early childhood. In addition, this non-invasive approach could delay the conventional food and thus save financial costs for more complex treatments. Finally, the installation of AS could afford, as demonstrated in adult teeth, lowering the cariogenic bacteria prevalence engaged in the caries process.

Main objective: To evaluate the effect of AS on caries incidence in the deciduous dentition obtained over a period of three years, taking into account the risk of caries established initially.

Secondary objectives:

1. To assess the prevalence and caries attack sites at the end of each year
2. Estimate the retention rate (partial or complete) of the AS during the study
3. Determine the cost savings of treatment during the trial period

Enrollment: 90 patients

Sex: All

Ages: 3 to 7 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Children who have at least two pairs (test / control) of healthy molars with occlusal surface or non cavitary initial injury.
• Children available for a follow-up 3 years
• Children being affiliated or beneficiary in a health insurance plan

Exclusion criteria

• Children involved in other research in the same field
• Child is exclusion period determined by previous research
• Children participating in research in the last three months its inclusion
• Parents do not understand French.
• Children deprived of liberty.
• Child participation Refusal
• Refusal to participate in either of the parents or legal representative

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: Single Blind

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90 participants in 2 patient groups

test tooth groups

Other group

Description:

test tooth groups

Treatment:

Other: decayed tooth surfaces

control tooth groups

Other group

Description:

control tooth groups

Treatment:

Other: decayed tooth surfaces