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Clinical Trials/NCT04694690
NCT04694690
Active, Not Recruiting
N/A

Clinical Performance of Resin Cements in the Adhesion of CAD/CAM Restorations

Hacettepe University1 site in 1 country53 target enrollmentNovember 20, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Restoration of Posterior Teeth
Sponsor
Hacettepe University
Enrollment
53
Locations
1
Primary Endpoint
Clinical performance
Status
Active, Not Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The clinical performance of different resin cements in adhesion of hybrid ceramic inlay and onlay restorations produced with CAD/CAM will be evaluated and compared. After obtaining a signed informed consent form from all the patients, all restorations will be placed by a single clinician. All hyrid ceramic restorations (Cerasmart, GC, Tokyo, Japan) will be produced using the same CAD/CAM CEREC Omnicam (Sirona Dental, Bensheim, Germany) system. 70 restorations will be divided into 2 groups: a self adhesive resin cement (RelyX U200 Automix, 3M ESPE, Seefeld, Germany), and an adhesive cement (G-Cem LinkForce, GC, Tokyo, Japan) which is applied after surface treatment (etch&rinse). All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after baseline, 6,12, 18, 24, 36 and 48 months. Descriptive statistics will be performed using Friedman test and Chi-square test.

Registry
clinicaltrials.gov
Start Date
November 20, 2018
End Date
August 20, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Simge Canatan

dentist

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • Healthy individuals with or without systemic disease
  • Patiens older than 18 years old
  • Good oral health
  • Patients who at least have1 large and deep carious lesion or broken restoration in a vital tooth
  • Patients who agreed to participate in the study after being informed about this study

Exclusion Criteria

  • Patient with periodontal disease
  • Patients with partial dentures
  • Patients with bruxism
  • Patients with malooclusion
  • Non vital or endodontically treated teeth
  • Preparetions under the cemento-enamel junction

Outcomes

Primary Outcomes

Clinical performance

Time Frame: 18 months

18 months- Modified United States Public Health Service

Study Sites (1)

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