Dentistry
Conditions
Interventions
Group 1: Non-invasive, milled restorations for patients with pathological loss of tooth structure.
A fully digital workflow is used as part of the study. If the pre-treatment has been completed, an
Sponsors
Prosec gGmbH
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: good knowledge of German, adults over 18 years of age, signed declaration of consent, pathological loss of dental hard tissue
Exclusion criteria
Exclusion criteria: Temporomandibular joint disorder, psychosomatically abnormal patients, pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Material wear of the tested material The wear behaviour of the restorative material is measured with the aid of intraoral scans directly after insertion as well as after 6, 12, 24 and 36 months after insertion. Furthermore, the colour stability is also measured intraorally using a spectrophotometer in addition to the above-mentioned data. The individual temporomandibular joint parameters are measured using a digital facebow. Questionnaires are used to evaluate the oral health-specific quality of life. All of this data is collected after integration and at the follow-up appointments. | — |
Secondary
| Measure | Time frame |
|---|---|
| Technical complications (chipping, fractures) | — |
Countries
Germany
Contacts
Public ContactElisabeth Prause
Charité-Universitätsmedizin Berlin
Outcome results
None listed