a preliminary safety study Occlusion, intraoral scanner, individual mandibular motion
Conditions
Interventions
Using intraoral scanner (TRIOS3) for recording Patient Specific Motion
Experimental Device
Sponsors
Mahidol University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Participants who have a complete permanent dentition with intact occlusal surfaces, absence of active carious lesions, or other tooth defects, 2. No signs of malocclusion and temporomandibular disorders, 3. Participants who have at least one of group function occlusion
Exclusion criteria
Exclusion criteria: 1. Unwillingness to participate in the study, 2. Presence of a parafunctional habit, 3. Participants who have third maxillary and mandibular molar or partially erupted tooth that interferes with normal occlusion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occlusal surface morphology at 3 months after end of the intervention 3D deviation | — |
Secondary
| Measure | Time frame |
|---|---|
| Remaining dentition at 3 months after end of the intervention 3D deviation | — |
Countries
Thailand
Contacts
Public ContactPanchanit Ouvorawong
Mahidol university
Outcome results
None listed