Status:
ACTIVE_NOT_RECRUITING
Clinical Comparison of Resin-hybrid Ceramic Restorations Produced Using a Computer-aided Design/Computer-aided Manufacturing (CAD/CAM) System With Fiber-reinforced Composite Restorations
Lead Sponsor:
Hacettepe University
Conditions:
Dental Caries
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The aim of this clinical study was to compare the clinical performance of CAD/CAM endochrone and fibre-reinforced composite restorations in root canal treated teeth with excessive loss.
Detailed Description
Restoration of endodontically treated teeth is one of the significant challenges encountered in dentistry. The restoration of these teeth is often confronted with a series of complex factors. Followin...
Eligibility Criteria
Inclusion
- Healthy individuals without any systemic disease
- Those between the ages of 18-65
- Individuals who brush their teeth twice a day
- Patients with at least 1 root canal treatment, loss of one or more tubercles and loss of at least 1 tooth wall in their posterior teeth after intraoral examination
- Tooth margins at gingival or supramarginal level
- Patients whose periodontal and endodontic treatments have been successfully completed and who do not show any subjective symptoms
- Voluntary individuals who agree to participate in the study and sign the informed consent form will be included in the study.
- Patients will be informed about the study, read the informed consent form and agree to be included in the study.
- Ability to apply rubber cover
Exclusion
- Individuals with uncontrolled systemic diseases
- Individuals with mental retardation who cannot co-operate
- Individuals with advanced periodontal disease
- Individuals using removable partial dentures
- Toothache, inadequate endodontic treatment or signs of periapical lesions on clinical examination or radiographic examination
- Vital teeth
- Individuals with bruxism
- Individuals with malocclusion
- Teeth with severe loss of material that requires extraction of the relevant tooth
- Patients read the informed consent form following the information about the study and did not agree to be included in the study
Key Trial Info
Start Date :
January 12 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 12 2025
Estimated Enrollment :
102 Patients enrolled
Trial Details
Trial ID
NCT06496126
Start Date
January 12 2023
End Date
April 12 2025
Last Update
July 11 2024
Active Locations (1)
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1
Hacettepe University
Ankara, Turkey (Türkiye), 06100