Evaluation of temporary cements regarding their biological interaction, esthetics and handling - a clinical prospective study
- Conditions
- Patients requiring dental crowns and fixed partial dentures
- Registration Number
- DRKS00024019
- Lead Sponsor
- VOCO GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
The length of the stump must be at least 3 mm (from the preparation margin to the functional incline); vital tooth
Exclusion Criteria
Allergy to components of the temporary cements;
allergy to temporary material;
pregnancy;
nursing mother;
age < 18 years;
non-consenting participant;
teeth prepared to receive anchorage for removable dentures;
teeth prepared to receive non-retentive partial crowns
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the following parameters are recorded before and after temporary restorations:<br>vitality of the tooth (positive/negative), percussion of the tooth (negative/positive), gingival bleeding index, odor formation in the temporary restoration
- Secondary Outcome Measures
Name Time Method during the temporary restoration, the manageability of the cement is assessed (simple, complicated) and after the temporary restoration the esthetics (inconspicuous, conspicuous)<br>all parameters are recorded in CRF questionnaires