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The aim of the study is :-
Full description
Total of 60 first permanent molar in male and female children aged between 6-9 years included in this prospective study will be selected randomly from the outpatient Pediatric Dentistry and Dental Public Health Department Faculty of Dentistry Ain Shams University.
Informed consent will be signed for each case by the patient's parent or guardian after thorough explanation of the study.
Procedural Steps:
In vivo
Group 1(Clinpro sealant)Active control
Group 2(Embrace WetBond sealant)
Group 3 (Fuji Triage sealant)
Articulating paper was used to check the occlusion and any premature contacts were adjusted. The patients were instructed not to eat or drink anything for 30 min, and not to bite or chew on hard substances for the rest of the day. The patients were recalled after a time interval of 1 and 6 months to evaluate the retention and development of caries using Modified Simonsen's criteria.
Criteria for evaluation: (Modified simonsen's criteria) Score 0: No loss of sealant and no evidence of caries Score 1: Partial loss of sealant and no evidence of caries Score 2: Partial loss of sealant and evidence of caries. Score 3: Complete loss of sealant and no evidence of caries Score 4: Complete loss of sealant and evidence of caries. On recall at 3 and 6th month interval, the sealants were evaluated by visual and tactile examination with a sharp probe for retention. The teeth were visually inspected for caries. The data obtained were tabulated and subjected to statistical analysis.
Enrollment
Sex
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Volunteers
Inclusion criteria
1- First permanent molars fully erupted with deep and retentive fissures,free of caries and free of any periapical radiolucency.
2- Males and Females 3- Age group between 6-9 years 4- Medically free 5- High caries risk children
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
100 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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