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Posterior Resin Bite Turbos Effect on Maxillary Expansion Using a HYRAX Expander in Early Adolescents

Effect of Posterior Disarticulatory Resin Bite Turbos on the Rate of Maxillary Expansion Using HYRAX Expander in Early Adolescent Patients: Randomized Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07739498
Acronym
HYRAX_ RME_SME
Enrollment
22
Registered
2026-07-31
Start date
2026-02-15
Completion date
2027-06-01
Last updated
2026-08-17

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

Conditions

Maxillary Transverse Deficiency (Posterior Crossbite) in Early Adolescent Patients

Keywords

Maxillary transverse deficiency - Rapid maxillary expansion - HYRAX expander - Bite turbos - Orthodontics - Intraoral scanning - RCT

Brief summary

This randomized controlled clinical trial aims to evaluate the effect of posterior disarticulatory resin bite turbos on the rate of maxillary expansion using a HYRAX expander in early adolescent patients. Participants will be randomly assigned to receive either maxillary expansion with posterior resin bite turbos or conventional expansion without bite turbos. The study will assess and compare the rate and effectiveness of maxillary expansion between the two groups during the treatment period. Clinical measurements will be recorded to evaluate skeletal and dental changes associated with the intervention.

Detailed description

This study is conducted as part of a Master's thesis in Orthodontics and aims to investigate the influence of posterior disarticulatory resin bite turbos on the rate of maxillary expansion achieved using a HYRAX expander in early adolescent patients. The study evaluates whether modifying occlusal contacts can affect skeletal and dental responses during rapid maxillary expansion. Participants will be monitored clinically throughout the expansion phase. Participants will be assigned in two groups: group 1: with posterior bite turbos group 2: without posterior bite turbos Digital intraoral scans will be taken on a weekly basis to assess changes in maxillary dimensions and to accurately measure the rate and pattern of expansion over time. These serial digital records provide high-resolution, non-invasive documentation of treatment progress. CBCT will be taken before the expansion and after retention phase for skeletal and dental measurement .

Interventions

DEVICEIntervention 1: HYRAX expander with posterior disarticulatory resin bite turbos

Description: Arm 1: Participants in this group receive a HYRAX rapid maxillary expansion appliance combined with posterior disarticulatory resin bite turbos. The bite turbos are placed on the posterior teeth to disclude the occlusion, aiming to reduce occlusal interference and potentially enhance skeletal response during maxillary expansion. The HYRAX appliance is activated according to a standardized expansion protocol.

DEVICEIntervention 2 (Control): HYRAX expander alone

Participants in this group receive a HYRAX rapid maxillary expansion appliance alone without the use of posterior bite turbos. The appliance is activated following the same standardized expansion protocol as the intervention group.

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

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

Intervention model description

This study is designed as a parallel-group randomized controlled clinical trial with two study arms. Participants are randomly allocated to receive either a HYRAX expander with posterior disarticulatory resin bite turbos or a HYRAX expander alone. Both groups are followed concurrently throughout the treatment period, and outcomes are assessed at predefined intervals using clinical evaluation and weekly digital intraoral scans to measure the rate of maxillary expansion.

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 10-14 years. 2. Bilateral posterior cross bite. 3. Functional lateral cross bite. 4. Good general and oral health. 5. Normal to decreased vertical height )average FMA 29.7 °± 4.2 °).23

Exclusion criteria

1. Patients with cleft lip and palate. 2. Severe facial asymmetry. 3. Anterior open bite. 4. Systemic conditions affecting tooth movement (e.g., diabetes, bone disorders). 5. Previous orthodontic treatment.

Design outcomes

Primary

MeasureTime frameDescription
The effect of occlusal disarticulation on the rate of maxillary expansion by linear measurements made on digital modelsBaseline and weekly during the active phase of expansion and after 3 months of retentionDental landmarks and measurements on models : d3 :Canine tip. d4: Central fissure of first premolar. d6 :Central fissure of first permanent molar. d\_3( inter canine width): Distance between left and right d3. d\_4 (inter first premolar width) : Distance between left and right d4. d\_6(inter first molar width): Distance between left and right d6.

Secondary

MeasureTime frameDescription
-The effect of the posterior disarticulation on alveolar bone changes by CBCT .baseline and after three months of retention after complete active expansionSkeletal transverse, vertical, nasal width changes and axial inclination of posterior teeth will be evaluated .
pain felt by the patient after activating the expansion screwfirst two weeks in active phase of expansionain will be assessed using the Visual Analogue Scale (VAS), a 100 mm line with "no pain" at the left end and "the worst unbearable pain" at the right, which corresponds to a pain score between 0 and 10. All participants will be asked to place a vertical mark indicating the level of pain on the VAS 4 h after each activation for the first two weeks in diary sheet containing the actual size of a 100mm of VAS. 25

Countries

Egypt

Contacts

CONTACTDonia Alashker
donyaalashker7@mans.edu.eg00201557372170
PRINCIPAL_INVESTIGATORDonia Alashker

Faculty of Dentistry Mansoura University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026