Posterior Resin Bite Turbos Effect on Maxillary Expansion Using a HYRAX Expander in Early Adolescents (HYRAX_ RME_SME)
Effect of Posterior Disarticulatory Resin Bite Turbos on the Rate of Maxillary Expansion Using HYRAX Expander in Early Adolescent Patients: Randomized Controlled Clinical Trial
Aperçu de l'étude
Statut
Description détaillée
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 .
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Donia Alashker
- Numéro de téléphone: 00201557372170
- E-mail: donyaalashker7@mans.edu.eg
Lieux d'étude
-
-
-
Al Mansurah, Egypte
- Recrutement
- Orthodontic Department - Faculty of Dentistry Mansoura University
-
Contact:
- Faculty of Dentistry Mansoura University
- Numéro de téléphone: 0020502267151
- E-mail: dentfac@mansoura.edu.eg
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
La description
Inclusion Criteria:
- Patients aged 10-14 years.
- Bilateral posterior cross bite.
- Functional lateral cross bite.
- Good general and oral health.
- Normal to decreased vertical height )average FMA 29.7 °± 4.2 °).23
Exclusion Criteria:
- Patients with cleft lip and palate.
- Severe facial asymmetry.
- Anterior open bite.
- Systemic conditions affecting tooth movement (e.g., diabetes, bone disorders).
- Previous orthodontic treatment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: group 1: HYRAX with posterior bite turbos
Participants in this arm receive a HYRAX rapid maxillary expansion appliance combined with posterior disarticulatory resin bite turbos.
The bite turbos are placed on posterior teeth to achieve occlusal disclusion, aiming to minimize occlusal interference during expansion and potentially enhance skeletal response.
The HYRAX expander is activated according to a standardized protocol throughout the treatment period, with regular follow-up using clinical assessment and weekly intraoral scans.
|
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. |
|
Comparateur actif: Group 2 : Expansion without posterior bite turbos
Participants in this arm receive a HYRAX rapid maxillary expansion appliance without the use of posterior disarticulatory resin bite turbos.
The appliance is activated according to a standardized expansion protocol similar to the experimental group.
Patients are followed throughout the treatment period with regular clinical assessments and weekly intraoral scans to monitor changes in maxillary dimensions.
|
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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The effect of occlusal disarticulation on the rate of maxillary expansion by linear measurements made on digital models
Délai: Baseline and weekly during the active phase of expansion and after 3 months of retention
|
Dental 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. |
Baseline and weekly during the active phase of expansion and after 3 months of retention
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
-The effect of the posterior disarticulation on alveolar bone changes by CBCT .
Délai: baseline and after three months of retention after complete active expansion
|
Skeletal transverse, vertical, nasal width changes and axial inclination of posterior teeth will be evaluated .
|
baseline and after three months of retention after complete active expansion
|
|
pain felt by the patient after activating the expansion screw
Délai: first two weeks in active phase of expansion
|
ain 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
|
first two weeks in active phase of expansion
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Donia Alashker, Faculty of Dentistry Mansoura University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- MS.26.02.145
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .