Evaluation of an Injectable Bioactive Restorative Material in children's molar teeth

Not Applicable

Recruiting

• Conditions: Dental caries; K02.9

• Registration Number: RBR-6b7b6tt
• Lead Sponsor: Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo (FORP-USP)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-10-17
• Last Update Posted: 29 May 2023
• Study Completion: 2024-01-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

The inclusion criterion will be that the patient must be between 4 and 8 years old; and have at least 2 homologous deciduous molars with caries lesions or fractures affecting only the occlusal or occlusal-proximal surfaces

Exclusion Criteria

Teeth with extensive structural loss requiring indirect restorations; endodontic treatment or indication for extraction; teeth with acute painful symptoms such as pulpitis or pericementitis; teeth with structural defects such as Molar-Incisor Hypomineralisation or Amelogenesis Imperfecta; children with parafunctional habits such as child bruxism

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluate the clinical behavior of an injectable single increment bioactive composite in deciduous molar restorations with the criteria approved by the World Dental Federation (FDI Criteria), at 1 week, 6 months and 12 months after restorations.

Secondary Outcome Measures

Name	Time	Method
Evaluate the survival curve of the restorations during the study period.