Effect of Carriere® Motion™ Appliance on Pharyngeal Airway Dimensions, Effect of Carriere® Motion™ Appliance on Skeletal and Dental Measurements
Conditions
Brief summary
Objectives: to evaluate the effect of treatment with Carriere® Motion™ Appliance on pharyngeal airway, skeletal and dental dimensions using lateral cephalometric radiographs and to compare these changes with a control group. Materials and Methods: a prospective controlled clinical study on 17 patients treated at King Abdulaziz university dental hospital, Jeddah, Saudi Arabia with a mean age of 15.25 ± 2.49 years with class II molar relationship (treatment group). They were treated with Carriere® Motion™ Appliance and initial and post treatment lateral cephalograms were taken to assess the effect of the appliance on the pharyngeal airway dimensions, skeletal and dental measurements. A matched sample of 18 untreated patients (with a mean age of 14.44 ± 2.25 years) acted as a control group. Independent sample T-test and paired T-tests were conducted. The significance level was set at P\< 0.05. Results: when the cephalometric changes associated with the treatment by Carriere® Motion™ Appliance were compared to the changes in the untreated control group, no significant differences were found between the groups in regard to the pharyngeal airway and the skeletal dimensions. The only significant difference between the two groups was in the proclination and the protrusion of the lower incisors. The treatment group showed significantly increased lower incisors proclination and protrusion (L1 to mand plane°= 3.38±2.6, L1-Apo= 0.99±1.45) compared to the control group (L1 to mand plane°=0.49±2.81, L1-Apo=0.39±1.86) (P\<0.05). Conclusion: treatment with Carriere® Motion™ Appliance does not have a significant effect on pharyngeal airway and skeletal dimensions. However, it significantly increases the lower incisors proclination and protrusion.
Interventions
DEVICECarriere® Motion™ Appliance
class II malocclusion corrector
Sponsors
King Abdulaziz University
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
12 Years to 20 Years
Healthy volunteers
No
Inclusion criteria
* Class II molar relationship. * Full set of teeth from 1st molar to 1st molar. * Age: between 12 and 20 years.
Exclusion criteria
* Craniofacial deformities. * Previous orthodontic treatment. * History of respiratory illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cephalometric pharyngeal airway changes (linear cephalometric measurements in mm) | For the treatment group: when class I molar relationship achieved. For the control group: not more than 18 months interval between the two lateral cephalograms. |
Secondary
| Measure | Time frame |
|---|---|
| skeletal and dental cephalometric changes (linear and angular cephalometric measurements) | For the treatment group: when class I molar relationship achieved. For the control group: not more than 18 months interval between the two lateral cephalograms. |
Countries
Saudi Arabia
Outcome results
None listed