Analysis of the Effect oh the Carriere Motion 3D

NCT ID: NCT06785896

Last Updated: 2025-01-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-07-11

Study Completion Date

2023-11-22

Brief Summary

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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."

Detailed Description

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Conditions

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Angle Class II

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Angle Class II unilateral, treated by carriere motion appliance

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

Angle Class II unilateral, treated by carriere motion appliance

Intervention Type PROCEDURE

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

Interventions

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Angle Class II unilateral, treated by carriere motion appliance

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

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

28 Years

Maximum Eligible Age

47 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nice

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU NICE

Nice, Alpes Maritimes, France

Site Status

Countries

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France

Other Identifiers

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24Odonto04

Identifier Type: -

Identifier Source: org_study_id

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