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NCT Number: NCT07608406

Modified Versus Clear Twin Block for Skeletal Class II Malocclusion

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.

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This study is active but is not currently recruiting participants.

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Key information

Age range

10 year–13 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Dentistry, University of Aleppo

Aleppo, Aleppo Governorate, Syria

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Modified Twin Block Appliance

Device

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.

Other names: Progressive Twin Block

Conventional Clear Twin Block Appliance

Device

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.

Other names: Clear Twin Block

Primary outcomes

  1. Change in mandibular skeletal position measured by SNB angle on lateral cephalometric radiographs

    Time frame: 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.

  2. Change in effective mandibular length measured by Co-Gn distance on lateral cephalometric radiographs

    Time frame: 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.

  3. Change in condylar dimensions assessed using cone-beam computed tomography (CBCT)

    Time frame: 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.

  4. Change in temporomandibular joint spaces assessed using CBCT

    Time frame: 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.

Secondary outcomes

  1. Temporomandibular joint dysfunction symptoms assessed using the Helkimo Anamnestic Index (Ai)

    Time frame: 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.
  2. Patient-reported pain intensity assessed using a Numeric Rating Scale (NRS)

    Time frame: 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.

  3. Patient-reported discomfort and functional limitation assessed using a validated questionnaire

    Time frame: 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.

  4. Change in lower incisor inclination measured by IMPA on lateral cephalometric radiographs

    Time frame: 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.

  5. Change in upper incisor inclination measured by U1-SN angle on lateral cephalometric radiographs

    Time frame: 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.

  6. Change in overjet measured on lateral cephalometric radiographs

    Time frame: 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.

  7. Change in overbite measured on lateral cephalometric radiographs

    Time frame: 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.

  8. Change in sagittal molar relationship measured on lateral cephalometric radiographs

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

University of Aleppo

Other

Registry information

Official study title

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

Acronym: MTB-CTB

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 27, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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