K08.1
Conditions
Interventions
Group 1: This is a mulitcentric prospective clinical study including 503 patients with 1013 implants. First they get a periodontal screening and the implantation followed by documentation of the EHI (
Sponsors
Universitätsklinikum Dresden, Poliklinik für Parodontologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients after tooth extraction which are able to get a dental implant.
Exclusion criteria
Exclusion criteria: Patients under 18 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint is defined as bone loss at the implant one year postimplantationem. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoint are biological- (BOP, pocket depth) and technical (implant system, implant- abutment- connection) factors influencing bone loss or periimplantitis. | — |
Countries
Germany
Contacts
Public ContactJörg- Ulf Wiegner
Saalepraxis, Praxis für Mund-, Kiefer- und Gesichtschirurgie
Outcome results
None listed