Viewing Study NCT04756349



Ignite Creation Date: 2024-05-06 @ 3:47 PM
Last Modification Date: 2024-10-26 @ 1:57 PM
Study NCT ID: NCT04756349
Status: COMPLETED
Last Update Posted: 2022-05-24
First Post: 2021-02-05

Brief Title: Clinical Performance of Adhesive Systems Containing HEMA and 10-MDP in Non Carious Cervical Lesions
Sponsor: Universidade Federal do Para
Organization: Universidade Federal do Para

Study Overview

Official Title: Clinical Performance of Adhesive Systems Containing HEMA and 10-MDP in Non Carious Cervical Lesions - A Two Years Randomized Double Blind Study
Status: COMPLETED
Status Verified Date: 2022-05
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 objective of this randomized double-blind clinical trial is to evaluate the clinical performance of non-carious cervicals adhesive restorations using three self-etching adhesives containing HEMA and 10-MDP monomers
Detailed Description: Sixty teeth n 20 for each group will be randomized into 03 groups Clearfil SE contains MDP and HEMA Optibond All-inOne contains HEMA and Prime and Bond Universal contains neither monomer dispatch Restorations will be performed by a single operator and no mechanical retention will be performed under the cavity After 6 12 and 24 months the restorations will be evaluated by two calibrated examiners using modified USPHS criteria for retention kappa 100 and adaptation marginal color kappa 081 and the results will be analysed by Fisher and Kruskal-Wallis respectively An intragroup analysis will be performed using the Cochran test for retention and Wilcoxon for marginal adaptation staining

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