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Clinical Comparison of Different Adhesives in NCCLs
Sponsor: Hacettepe University
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 etch\&rinse 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 etch\&rinse 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.
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
34
Start Date
2018-02-10
Completion Date
2026-06-10
Last Updated
2025-09-29
Healthy Volunteers
Yes
Conditions
Interventions
Clearfil Universal Bond Quick
Adhesive systems
Clearfil Universal Bond Quick
Adhesive systems
Clearfil Universal Bond Quick
Adhesive systems
Clearfil SE Bond
Adhesive systems
Tetric N-Bond
Adhesive systems
Locations (1)
Hacettepe University
Ankara, Turkey (Türkiye)