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CompletedNCT06785896Updated Jan 21, 2025

Analysis of the Effect oh the Carriere Motion 3D

An observational study in Angle Class II, sponsored by Centre Hospitalier Universitaire de Nice. Completed at 1 site in France. Open to participants aged 28 Years to 47 Years. Per ClinicalTrials.gov, last updated 2025-01-21.

Sponsored by Centre Hospitalier Universitaire de Nice · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
25
Ages
28 Years to 47 Years
Sex
All
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Study 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."

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Conditions studied

  • Angle Class II
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In context

Malocclusion, Angle Class II

124 studies on the registry are indexed under Malocclusion, Angle Class II; 19 are open to participants now.

Browse Malocclusion, Angle Class II studies →

Lead sponsor

Centre Hospitalier Universitaire de Nice is the lead sponsor of 723 studies on the registry; 176 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
28 Years to 47 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The study population consisted of patients treated by Dr. Romain de Papé at his practice in Strasbourg, within the established time frame.

Eligibility criteria

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

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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
25 participants (actual)
Patient registry
No

Groups and cohorts

  • Angle Class II unilateral, treated by carriere motion appliance

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

    Procedure: Angle Class II unilateral, treated by carriere motion appliance

Interventions

  • ProcedureAngle Class II unilateral, treated by carriere motion appliance

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

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What researchers measure

Primary outcomes

  1. Molar Angle class II correction

    Measured between the centro vestibular groove of the maxillar fisrt molar and the mesio vestibulair cusp tip of the mandibular molar in millimeters

    Time frame: Up to 6 months

Secondary outcomes

  1. Canine Angle class II correction

    Measurement performed between the maxillary canine cusp tip and the inter-dental space between the mandibular canine and premolar in millimeters

    Time frame: Up to 6 months

  2. Extrusion or intrusion

    Extrusion or intrusion of the maxillary canines and molars supporting the orthodontic appliance in millimeters

    Time frame: Up to 6 months

  3. Correction of the Class II canine relationship

    Mesured correction of the Class II canine relationship in millimeters

    Time frame: Up to 6 months

  4. Rotations

    Mesured of the Rotations of the molars and canines supporting the CMA in degrees

    Time frame: Up to 6 months

  5. Inter-incisal variations

    Mesure of the variation in the inter-incisal midline discrepancy in millimeters

    Time frame: Up to 6 months

  6. Arch depth

    Mesure of the variation in arch depth in millimeters

    Time frame: Up to 6 months

  7. Arch width

    Mesure of th variation in canine and molar arch width in millimeters

    Time frame: Up to 6 months

  8. Steiner analysis

    A Steiner analysis was performed on the lateral cephalograms, measurements in millimeters on the X-Ray

    Time frame: Up to 24 months

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Study locations

1 site
  • CHU NICE
    Nice, Alpes Maritimes 0600, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06785896
Responsible party
Sponsor
First posted
Jan 21, 2025
Start date
Jul 11, 2018
Primary completion
Nov 22, 2023
Completion
Nov 22, 2023
Last update
Jan 21, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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