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

Hacettepe University

Status: Active, not recruiting

Conditions: Tooth Diseases

Treatments: Device: Clearfil Univesal Bond; Device: G-Premio Bond; Device: IBond Universal

Study type: Interventional

Funder types: Other

Identifiers

NCT03415412

NCCLsclinic

Details and patient eligibility

About

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.

Enrollment: 18 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

18 participants in 3 patient groups

Group CU (Clearfil Universal)

Experimental group

Description:

Clearfil Univesal Bond (Kuraray Dental, New York, United States of America), adhesive system

Treatment:

Device: Clearfil Univesal Bond

Group IU (Ibond Universal)

Experimental group

Description:

IBond Universal (Heraeus Kulzer GmbH, Hanau, Germany), adhesive system

Treatment:

Device: IBond Universal

Group GP (G-Premio)

Experimental group

Description:

G-Premio Bond (GC Coorporation, Tokyo, Japan), adhesive system

Treatment:

Device: G-Premio Bond