Clinical Comparison of Resin-hybrid Ceramic Restorations Produced Using a Computer-aided Design/C… (NCT06496126) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Clinical Comparison of Resin-hybrid Ceramic Restorations Produced Using a Computer-aided Design/Computer-aided Manufacturing (CAD/CAM) System With Fiber-reinforced Composite Restorations
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.
Who can participate
Age range18 Years – 65 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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 Criteria:
* 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
What they're measuring
1
Retention
Timeframe: [Time Frame: From baseline to 24 month]
2
Marginal discoloration
Timeframe: [Time Frame: From baseline to 24 month]
3
Marginal Adaptation
Timeframe: [Time Frame: From baseline to 24 month]
4
Seconder Caries
Timeframe: [Time Frame: From baseline to 24 month]