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Evaluation of Two Protocol of Maxillary Protraction in Class III Adolescent After Using (MSE)

Evaluation of Two Protocol of Maxillary Protraction in Class III Adolescent After Using (MSE) Alt-RAMEC vs Conventional Rapid Palatal Expansion Randomized Controlled Trial -CBCT Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05489302
Enrollment
42
Registered
2022-08-05
Start date
2022-06-20
Completion date
2023-12-20
Last updated
2023-08-18

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

Conditions

Maxillary Protraction in Class III Adolescent After Using (MSE)

Keywords

Expansion, maxillary protraction, class III

Brief summary

The aim of this study of this study is to compare two protocol of maxillary protraction in class III adolescent after using (MSE) Alt-RAMEC vs conventional rapid palatal expansion using cone beam computed tomography (CBCT)

Interventions

DEVICEMaxillary skeletal expander with protraction face mask with Alt-RAMEC protocol.

The current study was conducted on a total sample of 21 young adult orthodontic patients presented with class 3 retrognathic maxilla with or without transverse maxillary deficiency by Alt-RAMEC protocol.

DEVICEMaxillary skeletal expander with protraction face mask with conventional protocol

The current study was conducted on a total sample of 21 young adult orthodontic patients presented with class 3 retrognathic maxilla with or without transverse maxillary deficiency by conventional protocol

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

* Class3 Patients suffering maxillary collapse with a skeletal background * Patients with retrognathic maxilla. * Patients with anterior cross-bite or incisor end-to-end relationship * Patients with unilateral or bilateral posterior crossbite. * Patients with no periodontal disease. * Patients with good oral hygiene and general health. * No systemic diseases that may affect bone quality or interfere with orthodontic treatment. * Patients with no previous orthodontic treatment.

Exclusion criteria

* previous orthodontic treatment. * Craniofacial syndrome.

Design outcomes

Primary

MeasureTime frameDescription
amount of maxillary protraction6 monthsprotraction of maxilla using CBCT

Countries

Egypt

Outcome results

None listed

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