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Analysis of the Effect oh the Carriere Motion 3D

Analysis of the Effect oh the Carriere Motion 3D on Patients With Class II Subdivision : a Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06785896
Enrollment
25
Registered
2025-01-21
Start date
2018-07-11
Completion date
2023-11-22
Last updated
2025-01-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angle Class II

Brief summary

Class II subdivision malocclusions are common and complex to treat due to their asymmetry. The range of orthodontic correction devices is expanding towards systems that are more comfortable for the patient but may not necessarily have scientific evidence to demonstrate their effectiveness. The aim of this study was therefore to evaluate, for the first time, the effect of a Class II correction device, namely the Carriere Motion 3D (CMA), on patients with a Class II subdivision malocclusion. Method:this retrospective observational study included all patients presenting with a Class II subdivision malocclusion and treated with CMA between July 2018 and November 2023. Before treatment (T0) and after treatment with CMA (T1), orthodontic data from dental molds and lateral cephalometric radiographs (Steiner analysis) were collected and statistically analyzed to assess dentoalveolar as well as skeletal effects of treatment using CMA.

Interventions

PROCEDUREAngle Class II unilateral, treated by carriere motion appliance

This treatment was unilateral, with dental composite bites ramps behind canines

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
28 Years to 47 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have completed their growth and present with a Class II subdivision malocclusion. * Patients who underwent orthodontic treatment with CMA between 07/11/2018 and 11/22/2023. * Patients who have a complete orthodontic record allowing for pre- and post-treatment measurements with CMA.

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frameDescription
Molar Angle class II correctionUp to 6 monthsMeasured between the centro vestibular groove of the maxillar fisrt molar and the mesio vestibulair cusp tip of the mandibular molar in millimeters

Secondary

MeasureTime frameDescription
RotationsUp to 6 monthsMesured of the Rotations of the molars and canines supporting the CMA in degrees
Inter-incisal variationsUp to 6 monthsMesure of the variation in the inter-incisal midline discrepancy in millimeters
Arch depthUp to 6 monthsMesure of the variation in arch depth in millimeters
Correction of the Class II canine relationshipUp to 6 monthsMesured correction of the Class II canine relationship in millimeters
Canine Angle class II correctionUp to 6 monthsMeasurement performed between the maxillary canine cusp tip and the inter-dental space between the mandibular canine and premolar in millimeters
Extrusion or intrusionUp to 6 monthsExtrusion or intrusion of the maxillary canines and molars supporting the orthodontic appliance in millimeters
Steiner analysisUp to 24 monthsA Steiner analysis was performed on the lateral cephalograms, measurements in millimeters on the X-Ray
Arch widthUp to 6 monthsMesure of th variation in canine and molar arch width in millimeters

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026