Clinical performance of two self-adhesive luting cements after 12 and 24 month
- Conditions
- uting of self-adhesive crowns/
- Registration Number
- DRKS00028276
- Lead Sponsor
- Justus-Liebig-Universität Gießen, ZZMK - Poliklinik für Zahnärztliche Prothetik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Subject is older than 18 years of age at time of enrollment
- Subject is in good general health
- Subject does not have known allergies against any study substances
- Subject is in need of a full coverage single crown on at least one tooth
- Subject volunteers to participate in the study
- Subject has an acceptable level of oral hygiene
- Subject has a vital study tooth or received a successful root canal treatment at least 6 month before restoration
- Subject lacks the capacity to consent to the research project and/or is unable to follow study instructions
- Subject is pregnant or breast feeding
- Subject has known allergies to any product used during study
- Study teeth with profound periodontitis
- Subject has a malignant tumor or has/ had a radiotherapy
- Subject has a drug or alcohol dependency
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of the study is restoration failure or loss of retention. Control is performed at T0, T1 and T2 during the clinical examination using USPHS criteria.
- Secondary Outcome Measures
Name Time Method Marginal adaptation, Marginal Discoloration, Secondary Caries, Tooth Vitality/ (Hyper) sensitivity