Efficacy of Sealing Molars: Split-mouth Randomized Clinical Trial
Primary Purpose
Dental Caries
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
High cost
Low Cost
Sponsored by
About this trial
This is an interventional treatment trial for Dental Caries focused on measuring dental caries, molars, Pit and Fissure Sealants
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.
Sites / Locations
- Faculty Sao Leopoldo MandicRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
High Cost
Low Cost
Arm Description
Restoration using a high-cost sealant
Restoration using a low-cost sealant
Outcomes
Primary Outcome Measures
Dental caries progression
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 Outcome Measures
Cost-effectiveness
The costs of each treatment procedure will be calculated and compared with thresholds values for intervention costeffectiveness by region, determined by World Health Organization (http://www.who.int/choice/costs/CER_levels/en/).
Impact on children's quality of life
The oral health related quality of life will be measured using a validated questionnaire according to the children's age. The "Early Childhood Oral Health Impact Scale" (ECOHIS) (Tesch et al., 2008) will be applied with 4-5 years old children. The "Child Perceptions Questionnaire" (CPQ) will be used for 6-9 years old children (Martins et al., 2009).
They will be applied immediately before the procedure and on 18 months follow-up and we will measure the difference between answers at baseline and the end of treatment (18months)
Children self-reported discomfort
The discomfort of each treatment will be evaluated using the facial scale of Wong-Baker (Wong, Baker, 1988). The patient will be asked to choose the face that is more similar to how he/she felt during the treatment. The answer should be given solely by the child, which means no parental or professional interferences. Each face corresponds to a number, within a numeric scale from 0 to 5, with 0 no discomfort and 5 the greatest discomfort. At the end, the averages of each score will be compared between the experimental groups.
Sealant retention
The elements submitted to the treatment will be codified in accordance with Hesse et al. (2012):
Full retention: When the restorer material was Intact when subjected to clinical examination;
Partial loss: When there was a loss of a part of the restorer material previously applied;
Total Loss: When the restorer material has been lost in its entirety.
Full Information
NCT ID
NCT03819868
First Posted
January 22, 2019
Last Updated
December 9, 2019
Sponsor
Faculty Sao Leopoldo Mandic Campinas
1. Study Identification
Unique Protocol Identification Number
NCT03819868
Brief Title
Efficacy of Sealing Molars: Split-mouth Randomized Clinical Trial
Official Title
Efficacy of Resin Sealing in Deciduous and Permanent Molars: Split-mouth Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 15, 2017 (Actual)
Primary Completion Date
February 15, 2019 (Actual)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Faculty Sao Leopoldo Mandic Campinas
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
Keywords
dental caries, molars, Pit and Fissure Sealants
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Split-mouth
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
High Cost
Arm Type
Active Comparator
Arm Description
Restoration using a high-cost sealant
Arm Title
Low Cost
Arm Type
Experimental
Arm Description
Restoration using a low-cost sealant
Intervention Type
Procedure
Intervention Name(s)
High cost
Intervention Description
Surfaces allocated to this group will be treated with a high-cost sealant (Fluroshield®, Dentsply, São Paulo, Brazil), according to the manufacturer's instructions.
Intervention Type
Procedure
Intervention Name(s)
Low Cost
Intervention Description
Surfaces allocated to this group will be treated with a low-cost sealant (Prevent®, FGM Produtos Odontológicos, Santa Catarina, Brazil), according to the manufacturer's instructions.
Primary Outcome Measure Information:
Title
Dental caries progression
Description
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.
Time Frame
Every 6 months up to 18 months
Secondary Outcome Measure Information:
Title
Cost-effectiveness
Description
The costs of each treatment procedure will be calculated and compared with thresholds values for intervention costeffectiveness by region, determined by World Health Organization (http://www.who.int/choice/costs/CER_levels/en/).
Time Frame
18 months
Title
Impact on children's quality of life
Description
The oral health related quality of life will be measured using a validated questionnaire according to the children's age. The "Early Childhood Oral Health Impact Scale" (ECOHIS) (Tesch et al., 2008) will be applied with 4-5 years old children. The "Child Perceptions Questionnaire" (CPQ) will be used for 6-9 years old children (Martins et al., 2009).
They will be applied immediately before the procedure and on 18 months follow-up and we will measure the difference between answers at baseline and the end of treatment (18months)
Time Frame
Baseline and 18 months
Title
Children self-reported discomfort
Description
The discomfort of each treatment will be evaluated using the facial scale of Wong-Baker (Wong, Baker, 1988). The patient will be asked to choose the face that is more similar to how he/she felt during the treatment. The answer should be given solely by the child, which means no parental or professional interferences. Each face corresponds to a number, within a numeric scale from 0 to 5, with 0 no discomfort and 5 the greatest discomfort. At the end, the averages of each score will be compared between the experimental groups.
Time Frame
Baseline
Title
Sealant retention
Description
The elements submitted to the treatment will be codified in accordance with Hesse et al. (2012):
Full retention: When the restorer material was Intact when subjected to clinical examination;
Partial loss: When there was a loss of a part of the restorer material previously applied;
Total Loss: When the restorer material has been lost in its entirety.
Time Frame
Every 6 months up to 18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
No
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jose Carlos P Imparato, PhD
Phone
+5511998686008
Email
jimparato@usp.br
Facility Information:
Facility Name
Faculty Sao Leopoldo Mandic
City
Campinas
State/Province
Sao Paulo
ZIP/Postal Code
13045755
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jose Carlos P Imparato, PhD
Phone
+551935183601
Email
jimparato@usp.br
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
24884684
Citation
Hesse D, Bonifacio CC, Mendes FM, Braga MM, Imparato JC, Raggio DP. Sealing versus partial caries removal in primary molars: a randomized clinical trial. BMC Oral Health. 2014 May 28;14:58. doi: 10.1186/1472-6831-14-58.
Results Reference
result
PubMed Identifier
19761288
Citation
Martins MT, Ferreira FM, Oliveira AC, Paiva SM, Vale MP, Allison PJ, Pordeus IA. Preliminary validation of the Brazilian version of the Child Perceptions Questionnaire 8-10. Eur J Paediatr Dent. 2009 Sep;10(3):135-40.
Results Reference
result
PubMed Identifier
18709230
Citation
Tesch FC, Oliveira BH, Leao A. [Semantic equivalence of the Brazilian version of the Early Childhood Oral Health Impact Scale]. Cad Saude Publica. 2008 Aug;24(8):1897-909. doi: 10.1590/s0102-311x2008000800018. Portuguese.
Results Reference
result
PubMed Identifier
3344163
Citation
Wong DL, Baker CM. Pain in children: comparison of assessment scales. Pediatr Nurs. 1988 Jan-Feb;14(1):9-17. No abstract available.
Results Reference
result
PubMed Identifier
22023543
Citation
Pitts N, Melo P, Martignon S, Ekstrand K, Ismail A. Caries risk assessment, diagnosis and synthesis in the context of a European Core Curriculum in Cariology. Eur J Dent Educ. 2011 Nov;15 Suppl 1:23-31. doi: 10.1111/j.1600-0579.2011.00711.x.
Results Reference
result
Learn more about this trial
Efficacy of Sealing Molars: Split-mouth Randomized Clinical Trial
We'll reach out to this number within 24 hrs