Caries Removal in Primary Teeth Using Er:YAG Laser
Dental Caries
About this trial
This is an interventional treatment trial for Dental Caries
Eligibility Criteria
Inclusion Criteria: Healthy patients between 9 and 12 years of age. Simple occlusal caries that is limited to enamel and dentine without proximal caries, or pulp involvement in at least two primary molars (pairs). Primary molars with 1/3rd of their root remained. Primary teeth have permanent successor teeth with 1/2 of the root formed. Exclusion Criteria: Caries lesion that had reached or was approaching the pulp. Previous fillings. Periapical lesions, or dental abscess. No permanent successor teeth. Behavioral or medical problem.
Sites / Locations
- King Abdulaziz University
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Er:YAG Laser Caries Removal group
Conventional Caries Removal Group
Complete isolation was performed using a rubber dam and saliva ejector. Patients received topical anesthesia before the clamp was placed. Dental caries was excavated using the Er:YAG laser with a wavelength of 2940nm according to the manufacturer's instructions until visual inspection showed that the carious lesions have been thoroughly removed. If the patient experienced pain and requested local anaesthesia, the procedure was stopped, local anaesthesia has been applied, and then the procedure has resumed. Cavities were restored using the Clearfil Universal Bond Quick system in total each mode; 37% phosphoric acid was used, then the Clearfil Universal Bond system was applied, light cured for 90 seconds, after which composite resin was applied (3M Filtek TM Z350 XT Universal Restorative Composite (3M ESPE) according to the manufacturer's instructions.
Complete isolation was performed using a rubber dam and saliva ejector. Patients received topical anesthesia before the clamp was placed. Dental caries was excavated using the Mastertorque high/low-speed air rotor handpiece until visual inspection showed that the carious lesions have been thoroughly removed. If the patient experienced pain and requested LA, the procedure was stopped, LA was applied, and then the procedure resumed. According to the manufacturer's instructions, cavities were restored using the Clearfil Universal Bond Quick system and composite resin (3M Filtek TM Z350 XT Universal Restorative Composite (3M ESPE).