Prospective clinical study to evaluate the performance of immediately loaded CERALOG Plus ceramic implants. A monocentric study
- Conditions
- K08.1Loss of teeth due to accident, extraction or local periodontal disease
- Registration Number
- DRKS00022174
- Lead Sponsor
- Zentrum der Zahn-, Mund- und KieferheilkundeCarolinum Zahnärztliches Universitäts-Institut gGmbHPoliklinik für Zahnärztliche Chirurgie und Implantologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 25
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.
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.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method