A randomized clinical trial to evaluate the safety and effectiveness of the full-veneer crown fabricated with a 3D printed resin material for definitive prosthesis
Not Applicable
Recruiting
- Conditions
- Codes for special purposes
- Registration Number
- KCT0006081
- Lead Sponsor
- Yonsei University Health System, Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
• Patients over 19 years of age
• Patients who have signed consent for clinical research
• Patients requiring single fixed posterior prosthetic treatment
• Patients without non-functional movements such as teething
• Patients without jaw joint and other occlusal disorders
• Patients whose opposing teeth are natural teeth
Exclusion Criteria
• Patients unable to read the consent
• Patients with uncontrolled systemic disease
• Patients with active lesions or symptoms on the tooth being restored
• patients with hypersensitivity to zirconia or resin materials
• patients who Inappropriate participation at the discretion of the principal investigator as it can affect the outcome of other ethical or clinical studies
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Inner surface and marginal fit of permanent prosthetic materials (photopolymerized resin) used in dental 3D printers
- Secondary Outcome Measures
Name Time Method Wear evaluation;Probing Depth, Bleeding on Probing;Gingival index;Fracture and crack inspection using a fluorescence test (Qray);Evaluation of the success rate of the prosthesis