Malocclusion K07.3
Conditions
Interventions
Group 1: Arm 1 - Patients in the test group are informed that the wearing time is being recorded.
Group 2: Arm 2 - Patients in the control group are only informed that the microsensor measures the tem
Sponsors
Poliklinik für Kieferorthopädie, LMU Klinikum
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1) consenting adults 2) indication for orthodontic treatment 3) malocclusion of teeth, either crowding or spacing
Exclusion criteria
Exclusion criteria: 1) dysgnathia; 2) craniofacial syndromes; 3) mental disorders; 4) diseases or dysfunctions affecting motor or cognitive abilities; 5) existence of dental implants.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is reached after the initial phase of the treatment period, i.e. after approximately three months and accordingly after 6 aligner changes. Up to this point, the wearing time (in hours/per day), number of treatment appointments, exact number of aligners, age and gender of the patients, place of treatment (clinic or practice) and health insurance status (private or statutory/self-payer) were recorded. | — |
Countries
Germany
Contacts
Public ContactJuliana Liedtke
Digitale Kieferorthopädie PullachDr. Fiona Adler
Outcome results
None listed