K08.1
Conditions
Interventions
Group 1: An intraoral scan of a propositus who is qualified for the study will be made three times without the resin splint. Then the trueness and precision of these digital impressions will be compar
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The propositus has at least one fully edentulous jaw or wide partial edentulous ridges where implants have been inserted to replace multiple missing teeth. The implants are osseointegrated, symptomless and, if necessary, exposured. A final implant-supported prosthesis is planned but has not yet been inserted. A gypsum master cast of the yaw with implant replicas generated by a conventional impression method is available.
Exclusion criteria
Exclusion criteria: The following proposituses are not included: - known tremor disease - epilepsy - disturbed nasal breathing - Allergy to the materials used in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Using splinted and unsplinted implant scan bodies, the primary outcome is to investigate the trueness of digital impressions of jaws or wide partial edentulous ridges where implants have been inserted. | — |
Secondary
| Measure | Time frame |
|---|---|
| Using splinted and unsplinted implant scan bodies, the secondary outcome is to investigate the precision of digital impressions of jaws or wide partial edentulous ridges where implants have been inserted. | — |
Countries
Germany
Contacts
Public ContactTabea Flügge
Universitätsklinikum Freiburg
Outcome results
None listed