Clinical Performance of regular resin composite with bioactive technology and resin-modified glass-ionomer in restorations of cervical lesions of Abfraction: a randomized controlled clinical trial

Not Applicable

• Conditions: Tooth Wear; C07.793.818

• Registration Number: RBR-5ntdwg
• Lead Sponsor: Faculdade de Odontologia de Bauru, Universidade de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-09-11
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Participants must be between 18 and 65 years of age; have good oral hygiene; absence of periodontal disease; have at least 20 teeth in occlusion and of these three or more teeth must present noncarious cervical lesions (NCL) of the abfraction type; the lesions should be approximately 2 mm deep.

Exclusion Criteria

Participants with caries activity; unsatisfactory oral hygiene conditions; severe bruxism or other parafunctional habits; periodontal disease and systemic complications; participants who have undergone orthodontic or hypersensitivity treatments in the past six months will be excluded; in addition to pregnant and lactating women; teeth with abfraction lesions that have an implant or total prosthesis as an antagonist will also not be included in the research.

Study & Design

• Study Type: Intervention
• Study Design: Not specified