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Effect of Modified Twin Block in Skeletal Class II Growing Females With Mandibular Deficiency

Primary Purpose

Class II Division 1 Malocclusion

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
twin block appliance
modified twin block appliance
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Class II Division 1 Malocclusion

Eligibility Criteria

9 Years - 12 Years (Child)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Skeletal Class II relationship (ANB > 4°).
  2. Mandibular retrognathy (SNB < 78°).
  3. Overjet ≥ 5 mm.
  4. Minimal crowding in dental arches (≤4 mm).
  5. Class II molar relation.
  6. Growing female patients.
  7. Patients with CMV3 maturation stage of the cervical verbrae.

Exclusion Criteria:

  1. No history of orthodontic treatment either prior to or during functional Appliance therapy.
  2. Posterior cross bites or severe maxillary transverse deficiency.
  3. Severe facial asymmetry determined by clinical or radiographical examination.
  4. Poor oral hygiene.
  5. Systemic diseases that may affect the orthodontic treatment results.
  6. Patients past their peak growth spurt.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    twin block appliance

    modified twin block appliance group

    Arm Description

    this group will receive conventional twin block appliance and followed up every month for 9 months.

    modified twin block appliance group , this group will receive the modified appliance and followed up every month for 9 months

    Outcomes

    Primary Outcome Measures

    enhancing mandibular skeletal growth
    it will be assessed by measuring the incremental growth by quick ceph (mm)

    Secondary Outcome Measures

    dentoalveolar changes
    quick ceph (mm)
    Improvement of soft tissue profile
    quick ceph (mm)
    Patient's compliance
    table chart (no of hours/day)

    Full Information

    First Posted
    August 15, 2018
    Last Updated
    November 30, 2018
    Sponsor
    Cairo University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03635463
    Brief Title
    Effect of Modified Twin Block in Skeletal Class II Growing Females With Mandibular Deficiency
    Official Title
    Effect of Modified Twin Block in Skeletal Class II Growing Females With Mandibular Deficiency: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2018 (Anticipated)
    Primary Completion Date
    December 2019 (Anticipated)
    Study Completion Date
    December 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cairo University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The aim of this study is to evaluate the treatment effects of conventional twin block appliance versus modified twin block appliance in the treatment of patients in growing stage having skeletal class II division 1 with mandibular deficiency.
    Detailed Description
    in this randomized controlled trail there are 2 groups , the first group will receive modified twin block appliance ,in the second group will receive conventional twin block appliance . the follow up period will be 9 months till mandibular growth occur . the assessment will be through a questionnaire on the number of hours the appliance is worn each day , and another questionnaire assessing the difficulty of speech and aesthetics . Also by, photographs, x-rays and study models preoperative and post operative.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Class II Division 1 Malocclusion

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Masking Description
    double blinded( participant and outcome assessor)
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    twin block appliance
    Arm Type
    Experimental
    Arm Description
    this group will receive conventional twin block appliance and followed up every month for 9 months.
    Arm Title
    modified twin block appliance group
    Arm Type
    Experimental
    Arm Description
    modified twin block appliance group , this group will receive the modified appliance and followed up every month for 9 months
    Intervention Type
    Device
    Intervention Name(s)
    twin block appliance
    Other Intervention Name(s)
    mandibular functional appliance
    Intervention Description
    a functional appliance that enhances mandibular growth in growing patients made from vaccum sheets (esthetic)
    Intervention Type
    Device
    Intervention Name(s)
    modified twin block appliance
    Intervention Description
    a convetional twin block functional appliance that enhances mandibular growth in growing patients
    Primary Outcome Measure Information:
    Title
    enhancing mandibular skeletal growth
    Description
    it will be assessed by measuring the incremental growth by quick ceph (mm)
    Time Frame
    9 months
    Secondary Outcome Measure Information:
    Title
    dentoalveolar changes
    Description
    quick ceph (mm)
    Time Frame
    9 months
    Title
    Improvement of soft tissue profile
    Description
    quick ceph (mm)
    Time Frame
    9 months
    Title
    Patient's compliance
    Description
    table chart (no of hours/day)
    Time Frame
    9 months

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    9 Years
    Maximum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Skeletal Class II relationship (ANB > 4°). Mandibular retrognathy (SNB < 78°). Overjet ≥ 5 mm. Minimal crowding in dental arches (≤4 mm). Class II molar relation. Growing female patients. Patients with CMV3 maturation stage of the cervical verbrae. Exclusion Criteria: No history of orthodontic treatment either prior to or during functional Appliance therapy. Posterior cross bites or severe maxillary transverse deficiency. Severe facial asymmetry determined by clinical or radiographical examination. Poor oral hygiene. Systemic diseases that may affect the orthodontic treatment results. Patients past their peak growth spurt.

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes

    Learn more about this trial

    Effect of Modified Twin Block in Skeletal Class II Growing Females With Mandibular Deficiency

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