Comparative analysis in implant-supported metal ceramic and hibrid ceramic crow
- Conditions
- Tooth LossC07.465.714.804
- Registration Number
- RBR-9w9m83
- Lead Sponsor
- Faculdade de Odontologia de Bauru
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Edentulous sites for replacement of unitary prostheses in the premolar or molar regions; bone height at least 8.5 mm; minimum cervical bone thickness of 5 mm; minimum age of 18 years; ASA I or ASA II patients; periodontally healthy adjacent teeth without previous treatment of chronic / aggressive periodontal disease and without the need for prosthetic restoration; healthy natural antagonist teeth (absence of restorations or prostheses) and periodontally healthy.
History of alcoholism; smokers; illicit drug users; cardiopathy; decompensated diabetics; complex rehabilitation needs (alteration of vertical dimension of occlusion, need for other rehabilitation procedures); lack of height and sufficient bone thickness; patients with parafunctional habits (bruxism); grafted areas; irradiated patients; patients who underwent long-term steroid therapy or bisphosphonate users; periodontally compromised patients.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome will be comparison of two restorative materials by analyzing the inflammatory markers, because there are values of these markers that represent health or disease of peri-implant tissue in the scientific literature . Success or failure will be determined by establishment of the disease or not, and the markers values present in the peri-implant fluid will be correlated with the clinical parameters assessed in the study.The evaluation periods will be: 3, 5, 9, 15, 30, 90, 180 and 360 days after implant placement.
- Secondary Outcome Measures
Name Time Method Secondary outcomes are not expected.