K00.2 K02.8 K02.9 K03.0 K03.1 K03.2 K03.6 K03.7 K03.8 K07.4 K08.0 K08.1 K08.9 K02.3 K00.4 K00.5 K00.8 K00.9
Conditions
Interventions
Group 1: Temporary restoration made of Protemp 4
Group 2: Temporary restoration made of Luxatemp® Automix Plus
Reference data, retrospective comparison
Sponsors
3M ESPE AG
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The study will include patients who are receiving a fixed partial denture or telescopic crowns, are at least 18 years old, have given informed consent
Exclusion criteria
Exclusion criteria: Patients who have a known allergy to constituents of the materials used, are addicted to medication, alcohol and/ or drugs, are suffering from infectious diseases (hepatitis, HIV, tuberculosis), are suffering from malignant tumors, are undergoing or have undergone radiotherapy, are pregnant or breast feeding, are not giving informed consent, are applying for renewal of a telescopic denture, that is already present
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the number of failures of the temporary restoration being made of Protemp 4 with the number of failures of temporary restorations being made of Luxatemp® Automix Plus (Reference data) | — |
Secondary
| Measure | Time frame |
|---|---|
| Colour stability, soft tissue reaction, clinical handling, accuracy of fit, outer shape, plaque accumulation, adhesion to the tooth stump and patients' opinion of the temporary restorations being made of Protemp 4 in comparison to the data of the temporary restorations being made of Luxatemp® Automix Plus (Reference data) | — |
Countries
Germany
Contacts
Public ContactBernd Wöstmann
Poliklinik für zahnärztliche Prothetik am Zentrum für Zahn-, Mund- und Kieferheilkunde der Uniklinik Gießen
Outcome results
None listed