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Clinical Trials/NCT03819868
NCT03819868
Unknown
Not Applicable

Efficacy of Resin Sealing in Deciduous and Permanent Molars: Split-mouth Randomized Clinical Trial

Faculty Sao Leopoldo Mandic Campinas1 site in 1 country200 target enrollmentAugust 15, 2017
ConditionsDental Caries

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Caries
Sponsor
Faculty Sao Leopoldo Mandic Campinas
Enrollment
200
Locations
1
Primary Endpoint
Dental caries progression
Last Updated
6 years ago

Overview

Brief Summary

The sealing of fossae and fissures is an effective procedure in preventing occlusal caries lesions. However, there are gaps regarding its efficacy in the treatment of initial enamel lesions. In addition, there are no studies in the literature that have compared the longevity of sealings performed with the different sealants available in the market. Thus, the objective of this study is to evaluate the efficacy of fossae and fissures sealings performed with a low-cost resinous sealant in occlusal lesions in enamel in permanent and deciduous molars. This is a multicenter clinical study of non-inferiority, randomized, controlled, double blind (patient and operator) with 60 deciduous molars and 340 permanent molars of children 4 and 9 years of age. The sample unit will be the tooth, which will be randomized into two groups using a distributed randomization list in mixed envelopes that will be open only at the time of the procedure. The teeth allocated in the test group will be treated with the sealant preventâ; Those allocated in the control group will employ the Fluroshieldâ sealant. In both groups the procedure will follow the manufacturer's standards. The efficacy of the sealant will be evaluated by means of clinical and radiographic control at 6, 12 and 18 months after the procedure. Secondary outcomes, such as retention, cost, acceptability and quality of life, will also be evaluated.

Registry
clinicaltrials.gov
Start Date
August 15, 2017
End Date
December 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Faculty Sao Leopoldo Mandic Campinas
Responsible Party
Principal Investigator
Principal Investigator

Jose Carlos P Imparato

PhD, Senior Lecturer, Clinical Professor

Faculty Sao Leopoldo Mandic Campinas

Eligibility Criteria

Inclusion Criteria

  • Children with at least two deciduous and/or permanent molars with occlusal caries lesions scores 1, 2 or 3 of the Icdas (Ismail et al., 2007) will be included, one on each side, preferably from the same arch.

Exclusion Criteria

  • Patients with special needs;
  • using orthodontic appliances;
  • with systemic diseases;
  • Teeth that present restorations, sealants, formation defects, deep caries lesions that may lead to pulp impairment;
  • teeth with fistula and/or abscess;
  • teeth with spontaneous painful symptomatology.

Outcomes

Primary Outcomes

Dental caries progression

Time Frame: Every 6 months up to 18 months

Caries progression will be evaluated radiographically by three previously trained evaluators (through theoretical classes and evaluation of 13 clinical photographs) and calibrated. These examiners will not know the chronological order and compare the images two to two first by two evaluators and when there is disagreement between the two, the third examiner shall be called for tie-breaker. The possible progression of the treated caries lesion will be codified as: * Present progression: Increased radiolucidity area of the Lesion * Absent progression: No increase in the area of radiolucidity of the lesion.

Secondary Outcomes

  • Cost-effectiveness(18 months)
  • Impact on children's quality of life(Baseline and 18 months)
  • Children self-reported discomfort(Baseline)
  • Sealant retention(Every 6 months up to 18 months)

Study Sites (1)

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