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Modified Versus Clear Twin Block for Skeletal Class II Malocclusion (MTB-CTB)

12 juli 2026 bijgewerkt door: Feras baba, University of Aleppo

Evaluation of the Efficacy of Functional Therapy Using Modified Twin Block Versus Clear Twin Block in Class II Skeletal Patients: A Randomized Controlled Clinical Trial

This study aims to evaluate the effectiveness of a modified Twin Block appliance compared to a conventional clear Twin Block appliance in the treatment of skeletal Class II malocclusion caused by mandibular retrusion in growing patients.

This is a two-arm randomized controlled clinical trial including patients aged 10-13 years diagnosed with skeletal Class II malocclusion. Participants will be randomly allocated into two equal groups.

Skeletal, dental, and soft tissue changes will be assessed using lateral cephalometric analysis and cone-beam computed tomography (CBCT). Additionally, temporomandibular joint (TMJ) health, pain perception, and functional tolerance will be evaluated using standardized clinical indices and patient-reported outcome measures.

The study aims to compare the modified appliance with the conventional design in terms of skeletal improvement, TMJ safety, and patient acceptance.

Studie Overzicht

Gedetailleerde beschrijving

Skeletal and dentofacial anomalies, particularly Class II malocclusion due to mandibular retrusion, represent one of the most prevalent orthodontic problems during growth. Functional appliances, especially the Twin Block appliance, are widely used to enhance mandibular development and correct jaw discrepancies. However, variations in treatment protocols, particularly regarding advancement mechanics and appliance modifications, may influence both skeletal outcomes and temporomandibular joint (TMJ) response.

This study aims to investigate the effects of a modified Twin Block appliance, incorporating progressive mandibular advancement and additional design modifications such as lower lip pads intended to influence muscular activity, compared to a conventional clear Twin Block appliance.

A two-arm randomized controlled trial will be conducted on growing patients aged 10-13 years diagnosed with skeletal Class II malocclusion due to mandibular retrusion. Participants will be randomly allocated into two equal groups using a computer-generated randomization sequence with allocation concealment.

Skeletal and dental changes will be evaluated using lateral cephalometric radiographs and cone-beam computed tomography (CBCT), with particular attention to condylar morphology, joint space dimensions, and craniofacial skeletal relationships. TMJ health will be assessed using the Helkimo Index. Patient comfort, pain perception, and functional adaptation will be evaluated using validated questionnaires administered at multiple time points throughout the treatment period.

Radiographic and clinical assessments will be performed at baseline (T0) and after 7 months of functional appliance therapy (T1). Repeated patient-reported outcome measures will be collected at predefined intervals during treatment.

The objective of this study is to determine whether the modified Twin Block appliance provides superior skeletal and functional outcomes while maintaining temporomandibular joint safety and improving patient tolerance compared to the conventional appliance.

Studietype

Ingrijpend

Inschrijving (Geschat)

40

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Aleppo Governorate
      • Aleppo, Aleppo Governorate, Syrië
        • Faculty of Dentistry, University of Aleppo

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Systemically healthy patients.
  • Patients willing to accept removable functional appliance therapy.
  • Skeletal Class II malocclusion (Angle Class II Division 1).
  • Skeletal Class II due to mandibular retrusion (ANB ≥ 5°, 6 mm ≤ OJ ≤ 13 mm , SNB ≤ 78°, with normal maxillary position).
  • Growth stage corresponding to MP3 stage or pre-pubertal peak according to hand-wrist radiograph (Björk and Helm, 1967).
  • No severe dental crowding in the dental arches and no significant maxillary dental protrusion.
  • Absence of congenital anomalies, trauma, burns, or surgical scars affecting the temporomandibular joint or craniofacial structures.
  • Absence of systemic or rheumatologic diseases affecting the temporomandibular joint.

Exclusion Criteria:

  • Presence of clinical signs or symptoms of temporomandibular joint disorders.
  • Functional mandibular deviation.
  • Previous orthodontic treatment.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Modified Twin Block Group
Patients in this group will be treated using a modified Twin Block appliance incorporating progressive mandibular advancement and lower lip pads designed to influence muscular activity and enhance skeletal effects.
A modified Twin Block functional appliance incorporating progressive mandibular advancement and lower lip pads designed to modify muscular activity and enhance mandibular growth. The appliance is used for the treatment of skeletal Class II malocclusion due to mandibular retrusion in growing patients.
Andere namen:
  • Progressive Twin Block
Actieve vergelijker: Conventional Clear Twin Block Group
Patients in this group will be treated using a conventional clear Twin Block functional appliance for correction of skeletal Class II malocclusion.
A conventional clear Twin Block functional appliance used for correction of skeletal Class II malocclusion in growing patients. The appliance acts by posturing the mandible forward to stimulate functional and skeletal adaptation.
Andere namen:
  • Clear Twin Block

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in mandibular skeletal position measured by SNB angle on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of sagittal mandibular skeletal position using the SNB angle (degrees) measured on standardized lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)
Change in effective mandibular length measured by Co-Gn distance on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of mandibular length using the Condylion-Gnathion (Co-Gn) linear measurement in millimeters obtained from lateral cephalometric analysis.
Baseline (T0) and after 7 months of treatment (T1)
Change in condylar dimensions assessed using cone-beam computed tomography (CBCT)
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of temporomandibular condylar morphology using CBCT, including condylar length, condylar width, and condylar height measured in millimeters.
Baseline (T0) and after 7 months of treatment (T1)
Change in temporomandibular joint spaces assessed using CBCT
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of condylar position within the glenoid fossa using CBCT measurements of anterior joint space (AJS), superior joint space (SJS), posterior joint space (PJS), and medial joint space (MJS), measured in millimeters.
Baseline (T0) and after 7 months of treatment (T1)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Temporomandibular joint dysfunction symptoms assessed using the Helkimo Anamnestic Index (Ai)
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)

Assessment of temporomandibular joint dysfunction symptoms using the Helkimo Anamnestic Index questionnaire. The index classifies patients into:

  • Ai0: no symptoms
  • Ai1: mild symptoms
  • Ai2: severe symptoms Higher scores indicate greater temporomandibular dysfunction severity.
Baseline (T0) and after 7 months of treatment (T1)
Patient-reported pain intensity assessed using a Numeric Rating Scale (NRS)
Tijdsspanne: 1 week, 2 weeks, 6 weeks, 3 months, and 6 months after appliance insertion
Assessment of pain intensity reported by patients using a numeric rating scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates maximum pain.
1 week, 2 weeks, 6 weeks, 3 months, and 6 months after appliance insertion
Patient-reported discomfort and functional limitation assessed using a validated questionnaire
Tijdsspanne: 1 week, 2 weeks, 6 weeks, 3 months, and 6 months after appliance insertion
Assessment of appliance-related discomfort and functional or social impairment using a validated questionnaire adapted from Sergl and Zentner (1998), modified by Idris et al. (2012). The questionnaire evaluates pressure sensation, tooth sensitivity, speech impairment, swallowing difficulty, mouth restriction sensation, and social confidence using a numeric rating scale from 0 to 10. Higher scores indicate greater discomfort and poorer appliance acceptance.
1 week, 2 weeks, 6 weeks, 3 months, and 6 months after appliance insertion
Change in lower incisor inclination measured by IMPA on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of lower incisor inclination using the Incisor Mandibular Plane Angle (IMPA) measured in degrees on lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)
Change in upper incisor inclination measured by U1-SN angle on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of upper incisor inclination using the upper incisor to SN plane angle (U1-SN) measured in degrees on lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)
Change in overjet measured on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of overjet as the horizontal distance between upper and lower incisors measured in millimeters on lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)
Change in overbite measured on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of overbite as the vertical overlap between upper and lower incisors measured in millimeters on lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)
Change in sagittal molar relationship measured on lateral cephalometric radiographs
Tijdsspanne: Baseline (T0) and after 7 months of treatment (T1)
Assessment of sagittal molar relationship using linear measurements in millimeters between upper and lower first molars on lateral cephalometric radiographs.
Baseline (T0) and after 7 months of treatment (T1)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Studie directeur: Abdulmalek Majanni, PhD, Faculty of Dentistry, University of Aleppo

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

17 mei 2026

Primaire voltooiing (Geschat)

1 december 2026

Studie voltooiing (Geschat)

1 december 2026

Studieregistratiedata

Eerst ingediend

12 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

20 mei 2026

Eerst geplaatst (Werkelijk)

27 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

14 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

12 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • MClearTB
  • UADS-3478-26052024/SRC-1994 (Andere identificatie: University of Aleppo Local Ethics Committee)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data will not be shared due to patient privacy and confidentiality considerations. The study involves pediatric orthodontic patients, and data will be reported in aggregate form only.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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