Performance of Glass-ionomer Cements: 2-year Follow-up
Primary Purpose
Dental Caries
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Glass ionomer
Glass ionomer cement
-Glass ionomer-
-Glass ionomer cement-
Sponsored by
About this trial
This is an interventional prevention trial for Dental Caries focused on measuring glass-ionomer cement, atraumatic restorative treatment, pit and fissure sealants
Eligibility Criteria
Inclusion Criteria:
- Volunteers that having at least two permanent first molars of opposite sides of the mouth, erupted in the oral cavity, caries-free and high-risk disease (presence of white spots, history of caries, plaque in smooth surfaces and gingivitis);
- Children who had one or two bilateral matched pairs of carious deciduous molars that required either class I or class II restorations.
Exclusion Criteria:
- Children who did not meet the minimum requirements for the achievement of sealants or parents / guardians did not agree to participate;
- No history of spontaneous pulpal pain.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Experimental
Active Comparator
Experimental
Arm Label
Ketac Molar® (3M/ESPE) - Glass ionomer
Maxxion® (FGM) - Glass ionomer cement
Ketac Molar® (3M/ESPE) - Glass ionomer -
Maxxion® (FGM) - Glass ionomer cement -
Arm Description
Pit and fissure sealing using conventional glass-ionomer cement
Pit and fissure sealing using conventional glass-ionomer cement
Restoration using conventional glass-ionomer cement
Restoration using conventional glass-ionomer cement
Outcomes
Primary Outcome Measures
Number of the teeth with glass-ionomer cement retention and prevention of caries.
Criteria established by Frencken et al. (1998) was used.
Number of the teeth with good restoration and caries absence.
Criteria established by Frencken et al. (1998) was used.
Secondary Outcome Measures
Frequency of loss of the sealing material and prevention of caries.
Criteria established by Frencken et al. (1998) was used.
Full Information
NCT ID
NCT02659917
First Posted
January 12, 2016
Last Updated
January 20, 2016
Sponsor
Fernanda Miori Pascon
1. Study Identification
Unique Protocol Identification Number
NCT02659917
Brief Title
Performance of Glass-ionomer Cements: 2-year Follow-up
Official Title
Performance of Glass-ionomer Cements in the Pit and Fissure Sealing and Atraumatic Restorative Treatment: a Randomized 2-year Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
August 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Fernanda Miori Pascon
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this randomized clinical trial was evaluate the performance of two conventional glass-ionomer cements in the pit and fissure sealing and atraumatic restorative treatment in high caries risk children.
Detailed Description
Sealants were applied on sound permanent first molars by "press finger technique" and carious deciduous molars that required either class I or class II restorations were restored according to manufacturers' recommendations in order to caries prevention and control.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
Keywords
glass-ionomer cement, atraumatic restorative treatment, pit and fissure sealants
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
147 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ketac Molar® (3M/ESPE) - Glass ionomer
Arm Type
Active Comparator
Arm Description
Pit and fissure sealing using conventional glass-ionomer cement
Arm Title
Maxxion® (FGM) - Glass ionomer cement
Arm Type
Experimental
Arm Description
Pit and fissure sealing using conventional glass-ionomer cement
Arm Title
Ketac Molar® (3M/ESPE) - Glass ionomer -
Arm Type
Active Comparator
Arm Description
Restoration using conventional glass-ionomer cement
Arm Title
Maxxion® (FGM) - Glass ionomer cement -
Arm Type
Experimental
Arm Description
Restoration using conventional glass-ionomer cement
Intervention Type
Other
Intervention Name(s)
Glass ionomer
Intervention Description
Application of preventive agent
Intervention Type
Other
Intervention Name(s)
Glass ionomer cement
Intervention Description
Application of preventive agent
Intervention Type
Other
Intervention Name(s)
-Glass ionomer-
Intervention Description
Atraumatic Restorative Treatment
Intervention Type
Other
Intervention Name(s)
-Glass ionomer cement-
Intervention Description
Atraumatic Restorative Treatment
Primary Outcome Measure Information:
Title
Number of the teeth with glass-ionomer cement retention and prevention of caries.
Description
Criteria established by Frencken et al. (1998) was used.
Time Frame
6-month
Title
Number of the teeth with good restoration and caries absence.
Description
Criteria established by Frencken et al. (1998) was used.
Time Frame
6-month
Secondary Outcome Measure Information:
Title
Frequency of loss of the sealing material and prevention of caries.
Description
Criteria established by Frencken et al. (1998) was used.
Time Frame
6-month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Volunteers that having at least two permanent first molars of opposite sides of the mouth, erupted in the oral cavity, caries-free and high-risk disease (presence of white spots, history of caries, plaque in smooth surfaces and gingivitis);
Children who had one or two bilateral matched pairs of carious deciduous molars that required either class I or class II restorations.
Exclusion Criteria:
Children who did not meet the minimum requirements for the achievement of sealants or parents / guardians did not agree to participate;
No history of spontaneous pulpal pain.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raquel V Rodrigues, PhD Student
Organizational Affiliation
Piracicaba Dental School - University of Campinas
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ana Carolina G Luciano, DDS
Organizational Affiliation
Piracicaba Dental School - University of Campinas
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kelly MS Moreira, MS Student
Organizational Affiliation
Piracicaba Dental School - University of Campinas
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Performance of Glass-ionomer Cements: 2-year Follow-up
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