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

2026년 7월 12일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

40

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
다른 이름들:
  • Progressive Twin Block
활성 비교기: 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.
다른 이름들:
  • Clear Twin Block

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in mandibular skeletal position measured by SNB angle on lateral cephalometric radiographs
기간: 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
기간: 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)
기간: 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
기간: 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)

2차 결과 측정

결과 측정
측정값 설명
기간
Temporomandibular joint dysfunction symptoms assessed using the Helkimo Anamnestic Index (Ai)
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Abdulmalek Majanni, PhD, Faculty of Dentistry, University of Aleppo

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 17일

기본 완료 (추정된)

2026년 12월 1일

연구 완료 (추정된)

2026년 12월 1일

연구 등록 날짜

최초 제출

2026년 5월 12일

QC 기준을 충족하는 최초 제출

2026년 5월 20일

처음 게시됨 (실제)

2026년 5월 27일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 12일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

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

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

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.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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