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Conditions
Interventions
3D printed and milled splints. 
Sponsors
Radboud Universitair Medisch Centrum
Eligibility
Age
16 Years to 64 Years
Inclusion criteria
Inclusion criteria: Subjects aged 18-45 yearsSubjects being healthy (ASA <IV)Subjects with healthy, complete dentitions (except for extractions of wisdom teeth, or tooth extractions for the purpose of orthodontic treatment in the past)Subjects willing and able to participate in the studySubjects willing to provide written informed consent for their participation in the study
Exclusion criteria
Exclusion criteria: Subjects with dental issues other than the inclusion criteriaSubjects with a history of autoimmune disorderSubjects with known allergies to acrylic materialsSubjects with severe allergies manifested by a history of anaphylaxis or those with severe, chronic allergies (e.g., asthma) and subjects with an active infection of any kind at the time of enrollmentSubjects who are pregnant or lactatingSubjects enrolled in another investigational clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assess the participant self reported findings regarding the comfort, retention, stability and fit of the milled and printed splint and in addition to the hygiene and discoloration of the splint over time. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assess the retention, stability and fit of the milled and printed splint by the dentist and assess the degree of wear of the different types of materials splints (printed/milled). | — |
Countries
Netherlands
Contacts
Public ContactS.L. Mechelse
Radboud Universitair Medisch Centrum
Outcome results
None listed