Prosthetic tooth improvement
Conditions
Interventions
Group 1: The prosthetic plan is first tried with a digitally designed conventional mock-up and then the virtual simulation is discussed.
Group 2: The prosthetic plan is first discussed with a digitall
Sponsors
Universität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahmedizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • complete upper dentition from 14-24 • seeking for an esthetic improvement in the upper front jaw • good general health and no systemic disease • periodontally healthy individuals • good oral hygiene • ability to comply with the study procedures • signed informed consent
Exclusion criteria
Exclusion criteria: • pregnancy, intention to become pregnant, breastfeeding, lack of safe contraception • medication or systemic disease with a contraindication for a prosthetic therapy • any active malignancy or patient undergoing treatment for malignancy • known or suspected non-compliance, drug or alcohol abuse • inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome will be the comparison of the OES-ratings changes between conventional mock-up and virtual mock-up at baseline (V1) and at the simulated treatment outcome (V3). | — |
Secondary
| Measure | Time frame |
|---|---|
| Demographics (V1) Time-measurement for the mock-up application and virtual simulation (V3) OES-rating at the end of the prosthetic treatment (V4) Costs (V2) | — |
Countries
Switzerland
Contacts
Public ContactAnina Zürcher
Universität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin
Outcome results
None listed