A randomized controlled pilot study evaluating efficacy, efficiency and patient-reported outcomes measures of single crown reconstructions
Not Applicable
- Conditions
- eed of a single crown in the posterior area
- Registration Number
- DRKS00019100
- Lead Sponsor
- niversität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
Signed Informed Consent form
- Need for a single crown in the posterior region of the maxilla or mandible
- Presence of an antagonist
- Presence of at least one neighboring tooth/implant
Exclusion Criteria
• Self-declared pregnancy or breast feeding at the date of inclusion
• Known or suspected non-compliance, drug or alcohol abuse
• Inability to follow the procedures of the study
• Smoking more than 15 cigarettes a day
• Poor oral hygiene after hygienic phase (Plaque Index > 30%)
• Active periodontal disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the chairside and the labside workflow after crown insertion in terms of esthetics as rated by patients
- Secondary Outcome Measures
Name Time Method Assessment regarding efficacy:<br>- Aesthetics as rated by the treating dentist <br>- Contact point, occlusion, marginal fit of the crowns <br><br>Assessment regarding efficiency:<br>- Number of appointments<br>- Treatment costs