TADs Anchored vs Conventional Anchored Carriere Motion Appliance

Al-Azhar University

Status: Completed

Conditions: Class II Malocclusion

Treatments: Device: Carriere Motion Appliance

Study type: Interventional

Funder types: Other

Identifiers

NCT05631353

Carriere motion appliance

Details and patient eligibility

About

Carriere Motion appliance (CMA) was designed to correct a Class II molar relationship into a Class I relationship by distalizing the whole posterior maxillary segment by means of class II elastics and mandibular anchorage. To revoke the adverse effects of CMA with class II elastics, we can use the CMA to distalize the maxillary posterior segment with TADs anchorage using miniscrews. The aim of this study is to evaluate TADs anchored CMA vs. conventionally anchored CMA for distalization of the maxillary buccal segment.

Full description

Twenty class II malocclusion patients with age (11-16) years will be randomly allocated in the two groups:

Group I: Patients will be treated by Carriere Motion Appliance using passive lingual arch.

Group II: Patients will be treated by Carriere Motion Appliance using direct mini-screw.

For each patient, two CBCT will be obtained: one preoperatively and another after completion of distalization.

Comparing skeletal and dental measurements obtained from CBCT radiographs obtained prior to treatment (T0) and immediately after correction of class II and remval of the appliance (T1).

Enrollment: 20 patients

Sex: All

Ages: 11 to 16 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Adolescent patients aged 11-17 years.
• Unilateral or bilateral Class II molar relationship.
• Bilateral Class II canine relationship.
• No history of previous orthodontic treatment.
• No malformed teeth, impacted teeth and unerupted teeth.
• No systemic disease.
• Good oral hygiene.
• No abnormal pressure habit.
• No periodontal diseases.
• No missing teeth in maxillary arch.

Exclusion criteria

• The need for extraction in the lower arch.
• Posterior crossbite.
• Presence of any craniofacial anomalies.
• Patients with syndromes.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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20 participants in 2 patient groups

Group I: Patients will be treated by Carriere Motion Appliance using passive lingual arch .

Active Comparator group

Description:

Conventional mandibular anchorage During the first month, 1/4-inch heavy elastics will be used. In the following months, 3/16-inch heavy elastics will be used. The patients will be instructed to wear the elastics 24 hours per day, except during mealtimes, and to change them daily

Treatment:

Device: Carriere Motion Appliance

Group II: Patients will be treated by Carriere Motion Appliance using direct mini-screw.

Active Comparator group

Description:

TADs mandibular anchorage. During the first month, 1/4-inch heavy elastics will be used. In the following months, 3/16-inch heavy elastics will be used. The patients will be instructed to wear the elastics 24 hours per day, except during mealtimes, and to change them daily

Treatment:

Device: Carriere Motion Appliance