Tooth Wear
Conditions
Brief summary
The aim of this randomized, controlled, prospective clinical trial is to evaluate the performances of two different universal adhesives and an etch&rinse adhesive in restoration of non-caries cervical lesions. Twenty patients will receive restorations. Lesions will be divided into 7 groups according to adhesive systems and application modes: GSE: Gluma Universal- self etch, GSL: Gluma Universal-selective etching, GER: Gluma Universal-etch&rinse, ASE: All Bond Universal- self etch, ASL: All Bond Universal- selective etching, AER: All Bond Universal- etch&rinse, SB (Control): Single Bond2+etch&rinse. Restorations (nano-hybrid 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.
Interventions
DEVICEGluma Universal
Adhesive systems
DEVICEAll Bond Universal
Adhesive systems
DRUGSingle Bond2
Adhesive systems
Sponsors
Hacettepe University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
Inclusion criteria will be as follows: 1. being 18 years or older, 2. having no medical or behavioral problems preventing then from attending review visits, 3. having at least 7 tooth with NCCLs (d) having antagonist teeth.
Exclusion criteria
Exlusion criteria will be: 1. poor gingival health, 2. uncontrolled, rampant caries, 3. bruxism, 4. removable partial dentures, 5. xerostomia.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical performances of different adhesives | Two years | Two year examinations according to USPHS criteria |
Outcome results
None listed