Ireland
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Recruiting Not applicable

Evaluation of Maxillary Expansion Methods on Nasomaxillary Structures

NCT07326345 · tracked via the Priya Life Science Turkey tracker
Sponsor
Merve Kulaksız
Phase
Not applicable
Started
2025-09-29
Last updated
2026-01-08

Condition(s) studied

Maxillary ExpansionMaxillary Transverse Deficiency

Investigational drug(s) / intervention(s)

MARPE (Mini-Screw Assisted Rapid Palatal Expansion)SARME (Surgically Assisted Rapid Maxillary Expansion)

MARPE (Mini-Screw Assisted Rapid Palatal Expansion): A mini-screw assisted rapid palatal expansion device used to achieve skeletal maxillary expansion through bicortical anchorage. The device delivers orthopedic forces to the maxillary sutures with reduced dental tipping and greater skeletal effects compared to conventional rapid palatal expansion appliances.

SARME (Surgically Assisted Rapid Maxillary Expansion): A surgically assisted maxillary expansion procedure performed to facilitate skeletal expansion in skeletally mature patients. The procedure involves weakening areas of resistance in the maxilla (e.g., lateral walls, midpalatal suture) followed by activation with a rapid palatal expansion device to achieve transverse maxillary widening.

Study summary

Maxillary transverse deficiency is an orthodontic anomaly characterized by the upper and lower dental arches being incompatible due to insufficient width of the maxilla. This condition typically manifests with clinical symptoms such as crossbite, crowding of teeth, and impaired respiratory function. Genetic factors, early primary tooth loss, mouth breathing, thumb sucking, and abnormal swallowing are among the causes of maxillary narrowing. Treatment options vary depending on the patient's age and the degree of suture closure. In pediatric and adolescent patients, rapid (RPE) or slow (SPE) orthodontic expansion can be achieved with palatal expansion appliances. However, in adult patients, due to the less flexible bone structure of the maxilla, methods such as surgically assisted expansion (SARME) or mini-screw-assisted expansion (MARPE) are preferred. Recent studies have shown that MARPE can be effective as a non-surgical alternative in young adults and can provide direct skeletal expansion without damaging the teeth.

Eligibility

Sex
ALL
Min age
15 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of maxillary transverse deficiency. * Patients aged 15 years and older. * Presence of unilateral or bilateral crossbite. Exclusion Criteria: * Severe facial deformities or craniofacial syndromes. * History of previous orthodontic treatment. * Existing pathology or history of surgery related to the paranasal sinuses, nasolacrimal system, or orbital cavity. * Inadequate patient cooperation. * History of trauma, or previous maxillofacial/plastic surgery procedures. * Clinical signs or symptoms of maxillary sinus pathology (e.g., maxillary sinus cysts, sinusitis).

Primary outcome measure(s)

  • Changes in Craniofacial Volumes — Cone-beam computed tomography (CBCT) scans will be obtained from patients in both groups at two specific time points: before the initiation of expansion treatment (T0) and following the 6-month retention period (T1).
    Evaluation of volumetric changes using CBCT analysis. Specific measurements include the total volume of the nasolacrimal and nasopalatine canals, maxillary sinus volume, and nasal airway volume.
  • Changes in Linear Dimensions of Canals and Ostium — Before expansion (T0) and after 6-month retention (T1).
    Assessment of linear changes including the anteroposterior and transverse diameters and lengths of the nasolacrimal and nasopalatine canals. Additionally, the diameter of the maxillary sinus ostium openings will be measured in millimeters.
  • Changes in Angulation and Septal Deviation — Cone-beam computed tomography (CBCT) scans will be obtained from patients in both groups at two specific time points: before the initiation of expansion treatment (T0) and following the 6-month retention period (T1).
    Assessment of angular changes in craniofacial structures. This includes the angulation of the nasolacrimal and nasopalatine canals and the degree of nasal septal deviation.

Trial sites (1)

FacilityCityRegionStatus
Bezmialem Vakif University Faculty of Dentistry, Department of Orthodontics Istanbul Fatih Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07326345 on ClinicalTrials.gov ↗ ← All trials in Turkey