DRKS00022174
Completed
Not Applicable
Prospective clinical study to evaluate the performance of immediately loaded CERALOG Plus ceramic implants. A monocentric study - CERALOG Plus
Zentrum der Zahn-, Mund- und KieferheilkundeCarolinum Zahnärztliches Universitäts-Institut gGmbHPoliklinik für Zahnärztliche Chirurgie und Implantologie0 sites25 target enrollmentJuly 1, 2020
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- K08.1
- Sponsor
- Zentrum der Zahn-, Mund- und KieferheilkundeCarolinum Zahnärztliches Universitäts-Institut gGmbHPoliklinik für Zahnärztliche Chirurgie und Implantologie
- Enrollment
- 25
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Voluntarily signed informed consent form before any study related action.
- •2\. Males and females with age at least 18 years old.
- •3\. Single tooth restorations in partially edentulous mandible and/or maxilla: single tooth gaps with sufficient bone for the placement of an implant with a diameter of 4\.5mm. Adjacent mesial and distal teeth must be natural teeth (roots).
- •4\. Tooth extraction at least 12 weeks prior to implant placement.
- •5\. Opposing dentition must be natural teeth or fixed restoration.
- •6\. Systematically healthy with no contraindications for oral surgical procedures.
- •7\. Patient has been informed of the follow\-up visits and is willing to return to the clinical center for these follow\-up visits.
Exclusion Criteria
- •1\. Smokers: \>10 cigarettes per day or cigar equivalents or chewing tobacco.
- •2\. Systemic disease that would interfere with dental implant therapy (e.g. uncontrolled diabetes).
- •3\. Uncontrolled para\-functional diseases (bruxism, clenching or grinding of teeth).
- •4\. Disorders that impede the ability of patients to maintain adequate oral hygiene.
- •5\. Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non\-compliance or unreliability.
- •6\. Pregnant or lactating women.
Outcomes
Primary Outcomes
Not specified
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