Okklusionsstörung
Conditions
Interventions
Group 1: This is a prospective clinical data collection study involving healthy adult subjects, in which the accuracy of conventionally collected occlusal contacts is compared with two different digit
Sponsors
Universitätsmedizin der Johannes Gutenberg Universität Mainz, Poliklinik für Kieferorthopädie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Only individuals between the ages of 18 and 40 will be considered for participation in the study. They must also be in good physical health, with no known acute or chronic illnesses, complaints or medical restrictions. There is no gender selection, so males, females and diverse individuals are eligible to participate.
Exclusion criteria
Exclusion criteria: All subjects who do not provide written consent or who have a pronounced gag reflex will be excluded from participation in the study. Subjects who are currently undergoing orthodontic treatment or who are under the minimum age of 18 will also be excluded. Furthermore, subjects with pronounced temporomandibular joint problems or diagnosed periodontitis will not be included.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of the study is to determine whether digital occlusion recording matches or exceeds the precision of conventional occlusion recording. | — |
Secondary
| Measure | Time frame |
|---|---|
| A secondary objective is to examine whether the type of digital bite registration used a) single-step occlusion registration (Primescan) or b) two-step occlusion registration (iTero) has an influence on digital reproduction accuracy. | — |
Countries
Germany
Contacts
Public ContactChristina Erbe
Universitätsmedizin der Johannes Gutenberg Universität Mainz, Poliklinik für Kieferorthopädie
Outcome results
None listed