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

2026年7月12日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

40

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Aleppo Governorate
      • Aleppo、Aleppo Governorate、シリア
        • Faculty of Dentistry, University of Aleppo

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
他の名前:
  • Progressive Twin Block
アクティブコンパレータ: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.
他の名前:
  • Clear Twin Block

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in mandibular skeletal position measured by SNB angle on lateral cephalometric radiographs
時間枠: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
時間枠: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)
時間枠: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
時間枠: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)

二次結果の測定

結果測定
メジャーの説明
時間枠
Temporomandibular joint dysfunction symptoms assessed using the Helkimo Anamnestic Index (Ai)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディディレクター:Abdulmalek Majanni, PhD、Faculty of Dentistry, University of Aleppo

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年5月17日

一次修了 (推定)

2026年12月1日

研究の完了 (推定)

2026年12月1日

試験登録日

最初に提出

2026年5月12日

QC基準を満たした最初の提出物

2026年5月20日

最初の投稿 (実際)

2026年5月27日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月14日

QC基準を満たした最後の更新が送信されました

2026年7月12日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • MClearTB
  • UADS-3478-26052024/SRC-1994 (その他の識別子:University of Aleppo Local Ethics Committee)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

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.

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いいえ

米国FDA規制機器製品の研究

いいえ

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