Efficiency of virtual versus conventional mock-ups in patient communication - a randomized controlled clinical trial in a cross-over desig
Not Applicable
Recruiting
- Conditions
- Prosthetic tooth improvement
- Registration Number
- DRKS00033419
- Lead Sponsor
- niversität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
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
•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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method Demographics (V1)<br>Time-measurement for the mock-up application and virtual simulation (V3)<br>OES-rating at the end of the prosthetic treatment (V4)<br>Costs (V2)<br>