Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age6-8
SponsorTanta University
About this trial
The aim of this study is to evaluate and compare the clinical effectiveness of ICON resin Infiltration versus conventional sealant and the microleakage and penetration depth of the two sealant materials.
Eligibility criteria
Qualifiers
Age of the children from 6 to 8 years.
Healthy children free from any systemic disease.
Show bilaterally sound fully erupted lower first permanent molars with deep narrow central fissures and supplemental grooves.
The eruption time of these molars should not exceed 3 years.
Disqualifiers
Children with fillings or sealants in the selected teeth.
Children with clinical evidence of caries in the selected teeth either white spot lesions or cavities.
Children with an allergy to any drug, such as resin restorative material.
Children with Extremely poor oral hygiene.
Trial design
Treatments tested in this trial
- ICON resin infiltration Material group in vivo
- Resin-based fissure sealant group in vivo
- ICON resin infiltration in vitro
- Resin-based fissure sealant in vitro
Treatment groups
86 Participants
are divided into 4 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov