Clinical Perfomance of regular resin composite with S-PRG technology and resin-modified glass-ionomer in restorations of Cervical Lesions with predominance of Abfraction: a randomized controlled clinical trial

Faculdade de Odontologia de Bauru, Universidade de São Paulo0 个研究点开始时间: 2020年9月11日最近更新: 2023年5月29日

适应症

试验速览

暂无简介。

•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.

•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.

发起方

Faculdade de Odontologia de Bauru, Universidade de São Paulo