Viewing Study NCT04481087



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Last Modification Date: 2024-10-26 @ 1:40 PM
Study NCT ID: NCT04481087
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2024-04-16
First Post: 2020-07-17

Brief Title: Clinical Comparison of Different Adhesives in NCCLs
Sponsor: Hacettepe University
Organization: Hacettepe University

Study Overview

Official Title: Clinical Comparison of Different Adhesives in NCCLs
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this randomized controlled prospective clinical trial is to evaluate the performances of a universal adhesive in three different application modes a self-etch adhesive and an etchrinse adhesive in restoration of non-caries cervical lesions Thirty-four patients will receive restorations Lesions will be divided into 5 groups according to adhesive systems and application modes CU-SE Clearfil Universal Bond Quick in self-etch mode CU-SLE Clearfil Universal Bond Quick in selective etch mode CU-ER Clearfil Universal Bond Quick in etchrinse mode CSE Clearfil SE Bond TB Tetric N-Bond Restorations Tetric N-Ceram composite will be scored with regard to retention marginal discoloration marginal adaptation recurrent caries and post operative sensitivity using modified USPHS criteria after 48 months Two examiners who is not involved in the placement of restorations will conduct the evaluations Descriptive statistics will be performed using Chi-square tests
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None