Cost-efficacy of Sealing Moderate Caries Lesions in Occlusal Surfaces of Primary Molars
Primary Purpose
Dental Caries
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Ionomer Restoration (control)
Ionomer Sealant (test)
Oral hygiene orientation and professional fluoride application
Sponsored by
About this trial
This is an interventional treatment trial for Dental Caries focused on measuring Dental Caries, Primary tooth, Ionomer Sealants, Glass Ionomer Restoration
Eligibility Criteria
Inclusion Criteria:
They will be included in this study children:
- aged 3 years and 6 years and 11 months;
- With complete primary dentition;
- Who have at least one active caries lesion score 3 or 4 ICDAS, in the occlusal molars surfaces.
- Who have assented to participate and whose parents have consented to their participation by signing the Instrument of Consent.
Exclusion Criteria:
- who have medical and / or behavioral conditions that require special considerations regarding handling / treatment;
- who are involved in other research that may impact on this study;
- whose parents that not agree in participate.
Sites / Locations
- University of São Paulo
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
restoration - control
sealant - test
Arm Description
Restoration
Sealant
Outcomes
Primary Outcome Measures
Need of reintervention
Need of reintervention will be considered as all failures after initial treatment that demand repair and/or caries progression associated to the treated lesion at baseline.
After cleaning, It will be analyzed the clinical evaluation of restorations and sealants, will be assessed the presence of caries lesions in dentin and / or evolution of ICDAS scores and if will be necessary other types of treatment, such as endodontics and extraction of teeth included.
Secondary Outcome Measures
Child's reported discomfort
The discomfort will be an outcome collected right after the end of treatment, using Wong baker scale
Duration of treatments
Time spent in interventions will be recorded.
Full Information
NCT ID
NCT03005405
First Posted
August 17, 2016
Last Updated
March 20, 2018
Sponsor
University of Sao Paulo
1. Study Identification
Unique Protocol Identification Number
NCT03005405
Brief Title
Cost-efficacy of Sealing Moderate Caries Lesions in Occlusal Surfaces of Primary Molars
Official Title
Cost-efficacy and Applicability of the Treatment of Moderate Caries Using Sealants as an Alternative to the Restorations on Occlusal Surfaces of Deciduous Teeth: a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This protocol aims to assess the cost-efficacy and applicability of the treatment of lesions moderate caries using sealants as an alternative to the restorations on occlusal surfaces of deciduous teeth. Initially, a non-inferiority study was designed in order to verify if sealing could be non-inferior than restoration. In this case, it could be preferable since it is less invasive. Therefore, cost will be put forward into the analysis considering even reintervention during the follow-ups (cost-efficacy analyses). Finally, the acceptability could be another differential point between treatments.
Detailed Description
This study aims to evaluate the cost-efficacy and applicability of the treatment of lesions moderate caries using sealants as an alternative to the restorations on occlusal surfaces of deciduous teeth. 96 children aged 3-6 years will be selected. Children must have at least one occlusal surface classified as scores 3 or 4 of International Caries Detection and Assessment System (ICDAS). Children will be randomly allocated according to the treatment: glass ionomer sealant and restoration with glass ionomer. After treatment, teeth will be assessed clinically after 6, 12, 18 and 24 months by trained and blinded examiners regarding the treatment received. The need of reintervention initially treated, either by failures that require repeating of the same procedure or for progression of caries lesions will be considered as primary outcomes. The secondary outcomes will be the chil's acceptability to the treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
Keywords
Dental Caries, Primary tooth, Ionomer Sealants, Glass Ionomer Restoration
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
96 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
restoration - control
Arm Type
Active Comparator
Arm Description
Restoration
Arm Title
sealant - test
Arm Type
Experimental
Arm Description
Sealant
Intervention Type
Procedure
Intervention Name(s)
Ionomer Restoration (control)
Other Intervention Name(s)
glass ionomer cement, restoration
Intervention Description
Restoration of moderate caries lesions after partial caries removal using high viscosity glass ionomer cements
Intervention Type
Procedure
Intervention Name(s)
Ionomer Sealant (test)
Other Intervention Name(s)
glass ionomer cement, sealant
Intervention Description
Sealing of moderate caries lesions without any caries removal or cavity opening.
Intervention Type
Procedure
Intervention Name(s)
Oral hygiene orientation and professional fluoride application
Intervention Description
Oral hygiene orientation and professional fluoride application
Primary Outcome Measure Information:
Title
Need of reintervention
Description
Need of reintervention will be considered as all failures after initial treatment that demand repair and/or caries progression associated to the treated lesion at baseline.
After cleaning, It will be analyzed the clinical evaluation of restorations and sealants, will be assessed the presence of caries lesions in dentin and / or evolution of ICDAS scores and if will be necessary other types of treatment, such as endodontics and extraction of teeth included.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Child's reported discomfort
Description
The discomfort will be an outcome collected right after the end of treatment, using Wong baker scale
Time Frame
1st day
Title
Duration of treatments
Description
Time spent in interventions will be recorded.
Time Frame
1st day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
They will be included in this study children:
aged 3 years and 6 years and 11 months;
With complete primary dentition;
Who have at least one active caries lesion score 3 or 4 ICDAS, in the occlusal molars surfaces.
Who have assented to participate and whose parents have consented to their participation by signing the Instrument of Consent.
Exclusion Criteria:
who have medical and / or behavioral conditions that require special considerations regarding handling / treatment;
who are involved in other research that may impact on this study;
whose parents that not agree in participate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mariana M Braga, PhD
Organizational Affiliation
University of São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of São Paulo
City
São Paulo
State/Province
SP
ZIP/Postal Code
05508-000
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Publication of all results, accessibility to data if necessary
Learn more about this trial
Cost-efficacy of Sealing Moderate Caries Lesions in Occlusal Surfaces of Primary Molars
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