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Clinical Trial Summary

evaluate the clinical performance of EQUIA Forte ® ( a HVGIC) and Plafique® Bulk Flow composite resin when placed in class II cavities in primary molars.


Clinical Trial Description

1. Thorough diagnosis of patients will be done by the primary investigator. Patients with class II carious primary molars with score 4 or 5 using the International Caries Detections and Assessment Criteria (ICDAS). 2. Pre-operative bitewing radiographs will be obtained to assess the depth of the cavity. Primary molars with score D1 or D2 according to the ADA will be included in the study. 3. Each patient will be assigned to one of the two groups. - Group I (n= 59): Plafique Bulk Flow Composite. - Group II (n=59): EQUIA Forte Group. 4. Class II carious primary molars are prepared using 330 burs. The cavity will be approximately with a depth of 0.5 mm in dentin and width of at least one-third of the occlusal table. Outline of the cavity will be determined by the extent of the carious lesion. No beveling will be done in any of the cavities. 5. Matrix is placed and secured in position. 6. One of the 2 restorative materials is placed in the cavity using the manufacturer's instructions. 7. Patients will be recalled at 3, 6, and 12 months to evaluate the restoration clinically using the FDI criteria. 8. Patients will receive oral health education on how to maintain a proper oral hygiene and proper diet consumption. 9. They will be given manual tooth brushes and tooth pastes to use during the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06235489
Study type Interventional
Source Ain Shams University
Contact Mariam M Abdel Azim, Ass. Lec
Phone 0122841611
Email mariam.m.abdelazim@dent.asu.edu.eg
Status Recruiting
Phase N/A
Start date June 1, 2022
Completion date May 1, 2024

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