Malocclusion
Conditions
Interventions
This is a two-arm randomized controlled clinical study. Group 1 - control: 15 patients will wear Invisalign orthodontic aligners for a period of 22 hours a day. Group 2 - evaluation: 15 patients will
Sponsors
Faculdade de Odontologia de Bauru da Universidade de São Paulo
Faculdade de Odontologia de Bauru da Universidade de São Paulo
Eligibility
Age
14 Years to 60 Years
Inclusion criteria
Inclusion criteria: Participants aged between 14 and 60; both sexes; complete permanent dentition; Angle Class I; good periodontal health; mild to moderate malloclusion
Exclusion criteria
Exclusion criteria: Patients with incisive agenesis; dental losses (except third molars); or indication of premolar extraction for orthodontic purposes
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effectiveness of different daily protocols for the use of aligners, 10 hours and 22 hours, by assessing the dissolution of the patients' dental crowding in each of these periods, based on a variation of less than 5% post-intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the durability of 2 fluid resins (conventional and with load) in the manufacture of attachments by evaluating their resistance during treatment, seeking a variation of less than 5% post-intervention | — |
Countries
Brazil
Contacts
Public ContactCássia Rubira
Faculdade de Odontologia de Bauru da Universidade de São Paulo
Outcome results
None listed