Clinical Evaluation of Three Different Universal Adhesives in Non-carious Cervical Lesions

Not Applicable

Active, not recruiting

• Conditions: Tooth Diseases
• Interventions: Device: G-Premio Bond; Device: Clearfil Univesal Bond; Device: IBond Universal

• Registration Number: NCT03415412
• Lead Sponsor: Hacettepe University

Brief Summary

The aim of this randomized, controlled prospective clinical trial is to evaluate and compare the performances of three different universal adhesives using a flowable universal composite resin in the restoration of non-caries cervical lesions over 48-month period.Participants over 18 will be included to the study. Oral hygiene instructions will be given before procedures. All the lesions will be restored by the same clinician who will not participate to the selection of patients for eligibility. Each patient will receive at least three restorations and randomization will be applied using a table of random numbers. All lesions will be cleaned before restoring. Adhesive procedures and restorations will be placed according to manufacturers' recommandation.

The flowable universal composite resin will be placed in bulk and light-cured for 40 seconds. The restorations will be contoured and polished with Optidisc discs (Kerr Coorporation, Orange, CA, USA).

Patients will be recalled at baseline and will be recalled at control periods after placement.

Detailed Description

Not available

Study Timeline

• Study Start: 2016-04-01
• Primary Completion: 2016-06-01
• Study First Submitted: 2017-12-23
• Study First Submitted QC: 2018-01-28
• Study First Posted: 2018-01-30
• Status Verified: 2024-08
• Last Update Submitted: 2024-08-21
• Last Update Posted: 2024-08-22
• Study Completion: 2025-06-01

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

• 18 years old with 20 teeth under occlusion. They will be required to have at least three NCCLs needed restoration in different teeth. All the NCCLs selected were in similar sizes varying between 1-3 mm.

Exclusion Criteria

• Patients with severe periodontal disease, rampant, uncontrolled caries, xerostomia, serious medical problems preventing them from attending review visits, poor gingival health, heavy bruxism and removable partial dentures will not be included in the present study. Also, participiants will be excluded, if they are undergoing bleaching treatment or orthodontic treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group GP (G-Premio)	G-Premio Bond	G-Premio Bond (GC Coorporation, Tokyo, Japan), adhesive system
Group CU (Clearfil Universal)	Clearfil Univesal Bond	Clearfil Univesal Bond (Kuraray Dental, New York, United States of America), adhesive system
Group IU (Ibond Universal)	IBond Universal	IBond Universal (Heraeus Kulzer GmbH, Hanau, Germany), adhesive system

Primary Outcome Measures

Name	Time	Method
Clinical performances of different universal adhesives	Two years	Two year results according to USPHS criteria