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Three-dimensionally Printed Hyrax Versus Conventional Hyrax for Maxillary Arch Expansion in Adolescents

Three-dimensionally Printed Hyrax Versus Conventional Hyrax for Maxillary Arch Expansion in Adolescents: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07411092
Enrollment
22
Registered
2026-02-13
Start date
2025-08-01
Completion date
2027-01-01
Last updated
2026-02-13

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

Conditions

Maxillary Expansion, Transverse Maxillary Deficiency

Keywords

Maxillary Expansion, Hyrax expander

Brief summary

This clinical trial aims to compare the skeletal and dental effects of conventional Hyrax expanders and 3D-printed Hyrax expanders in adolescent patients with maxillary transverse deficiency. Using cone-beam computed tomography (CBCT) and digital models, the study evaluates the precision, customization, and treatment outcomes of both appliance types to inform evidence-based orthodontic treatment planning.

Detailed description

Maxillary transverse deficiency is a common orthodontic problem that often requires skeletal expansion using appliances such as the Hyrax expander. While conventional Hyrax expanders have been widely used, advancements in digital dentistry have introduced 3D-printed alternatives that offer potential benefits in precision, customization, and patient comfort. However, there is currently no clinical evidence comparing the skeletal and dental effects of these two designs. This study addresses this gap by evaluating and comparing the outcomes of conventional and 3D-printed Hyrax expanders in adolescent patients, a critical developmental stage where maxillary expansion becomes more challenging due to progressive maturation and increased resistance of the mid-palatal suture. The study uses cone-beam computed tomography (CBCT) and digital models to assess skeletal and dental changes, providing clinically relevant data to guide orthodontic treatment planning and appliance selection.

Interventions

DEVICEThree dimensionally printed hyrax expander

Group A : A 3D-printed Hyrax expander designed for rapid maxillary expansion in orthodontic treatment. The device is manufactured using additive manufacturing technology for a customized fit.

DEVICEConventionally Fabricated Hyrax Expander

Group B: A conventionally fabricated Hyrax expander used for rapid maxillary expansion . The device is made using traditional laboratory techniques.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

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

Inclusion criteria

1. Patients aged between 12 to 17 years. 2. Skeletal age ranges from CVMS 3 to CVMS 5. 3. Skeletal maxillary transverse deficiency with/without crossbite. 4. Cooperative and able to attend follow-up visits.

Exclusion criteria

1. Previous orthodontic treatment. 2. Craniofacial syndromes, or cleft lip and/or palate. 3. Patients with vertical growth pattern. 4. Very bad oral hygiene and active periodontal disease. 5. Vulnerable groups such as individuals with cognitive impairments or intellectual disabilities and individuals with severe mental health disorders.

Design outcomes

Primary

MeasureTime frameDescription
Amount of mid-palatal suture opening.Three weeksThe amount of suture separation measured in millimeters in the axial plane through CBCT X-ray

Secondary

MeasureTime frameDescription
Amount of dental expansionThree weeksDental expansion will be measured as changes in inter-canine width and intermolar width (in millimeters) on digital dental models.
The amount of tipping of maxillary molars and premolars.Three weeksBuccolingual tipping of maxillary molars and premolars will be quantified as angular changes measured on CBCT by comparing pre-expansion and post-expansion images.
Change of buccal alveolar bone thickness.Three weeksChanges in buccal alveolar bone thickness in millimeters will be measured on pre-expansion and post-expansion CBCT scans.
Pain assessmentThree weeksEvaluating the pain experienced during the active expansion phase using the Visual Analogue Scale (VAS; 0-100 mm), where 0 mm represents no pain and 100 mm represents the worst imaginable pain; the higher the value in the VAS scale, the more severe the pain.
Oral health-related quality of life.Three weeksOral health-related quality of life was assessed using the Oral Health Impact Profile-14 (OHIP-14). Items are rated on a 5-point Likert scale (0 = never to 4 = very often). Results are presented as mean scores (0-4); higher values indicate worse oral health-related quality of life.
Stability of transverse skeletal width at 6 months post-expansionSix monthsThe transverse skeletal dimension after appliance removal after six months post-expansion will be measured in the axial plane on the CBCT X-ray.

Countries

Egypt

Contacts

CONTACTSara S Mandour, Msc, Assistant lecturer
sarasaleh@dent.asu.edu.eg+201061531431
CONTACTMarwah S Abdel-Latif, Msc, PHD, Lecturer
marwahsalah@asfd.asu.edu.eg+201002955774

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026