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Clinical Trial Summary

to evaluate and compare the clinical performance and periodontal responses of four commercially available one-step universal adhesives with different formulations in Class II composite restorations over a three-year period.


Clinical Trial Description

The experimental design description adhered to the guidelines provided by the Consolidated Standards of Reporting Trials (CONSORT) statement. The present study is planned as a double-blinded randomized clinical trial, ensuring that both the patients and the examiner are unaware of the treatment allocation. The trial will follow a split-mouth design. A total of forty-eight adult patients, who are seeking dental treatment, will be enrolled in the study. The participants will be recruited from the Outpatient clinic at Faculty of Dentistry, Mansoura University. No active advertisement will be used for participant recruitment, and instead, a convenience sample will be formed. Prior to participating in the study, each patient will be required to provide informed consent by signing a consent form. The protocol of the study was approved by Mansoura University's ethics committee before initiation ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06265116
Study type Interventional
Source Mansoura University
Contact Omar A Abd El-Maksoud
Phone 01024366555
Email omarabdelfata7.92@gmail.com
Status Recruiting
Phase N/A
Start date January 23, 2024
Completion date January 30, 2027

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