Retention of implant-supported single crowns K08.1
Conditions
Interventions
Group 1: standard abutment
Group 2: individual abutment
Sponsors
Universitätsklinikum Heidelberg
Mund-Zahn-Kieferklinik, MZK II
Poliklinik für Zahnärztliche Prothetik
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria consist of signing the informed consent, being in the age of 18-100 and legally competent. Only patients with a bonelevel-implant, that is osseointegrated and has no clinical signs of inflammation will be included. Patient must be informed in detail about the treatment procedure, the randomization and the costs.
Exclusion criteria
Exclusion criteria: Exclusion criteria are: vulnerable patients, pregnancy or brestfed, patients with tissue level implants or bonelevel implants that have clinical signs of mucositis or periimplantitis, missing informed consent, refusing the randomization and patients with bisphosphonates or radiation therapy in the head or neck area.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is to examine the undetected excess cement on standard and individual abutments after 2 weeks (explorative examination). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are the examination of the periimplant soft tissue for volumetric changes or signs of inflammation, and cases of loss of retention will also be documented. | — |
Countries
Germany
Contacts
Public ContactStefanie Kappel
Universitätsklinikum Heidelberg Mund-Zahn-Kieferklinik, MZK II Poliklinik für Zahnärztliche Prothetik
Outcome results
None listed