search
Back to results

Comparison of Efficacy of Three Orthodontic Appliances

Primary Purpose

Malocclusion, Angle Class II

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Twin Block, Herbst, Frog distalising appliance
Sponsored by
Guy's and St Thomas' NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malocclusion, Angle Class II

Eligibility Criteria

10 Years - 16 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Patients aged 10-16 years of age in the late mixed/permanent dentition with Class II malocclusions (Both Cl II div 1 and Cl II div 2)
  2. > 1/2 unit Class II molar relationship bilaterally (at least 3.5mm)
  3. Normal or deep overbite cases will be included
  4. Skeletal Class II relationship (ANB > 4°)
  5. Overjet ≥ 5 mm in Cl II/1 cases
  6. Non-extraction cases

Exclusion Criteria:

  1. Children in the early mixed dentition
  2. Class I and Class III malocclusions
  3. Malocclusions with less than 1/2 unit II molar relationship
  4. Reduced overbite / anterior openbite
  5. Medically compromised patients, syndromic patients or patients with severe facial asymmetry
  6. Special needs patients not able to comply with instructions / difficulty with compliance
  7. Hypodontia or extracted permanent tooth (except third molars)
  8. Poor oral hygiene with both Gingival bleeding Index and Plaque Index scoring no more than 1

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Active Comparator

    Active Comparator

    Arm Label

    Twin Block

    Herbst

    Frog distalising appliance

    Arm Description

    61 patients will receive the Twin Block appliance (one of the three appliances being studied)

    61 patients will receive the Herbst appliance (one of the three appliances being studied)

    61 patients will receive the Frog distalising appliance (one of the three appliances being studied)

    Outcomes

    Primary Outcome Measures

    Number of participants who have experienced discomfort related to wearing the appliance
    This is to check which appliance produces more discomfort compared to the other appliances using the Likert scale. Each question on the scale asks to rate the pain as either (no pain, slight pain, moderate pain, severe pain) or (strongly disagree, disagree, agree, strongly agree). Patients will choose a response which matches their experience.
    establishing which appliance has the fastest completion time
    The three appliances will be compared in 'months' from the start of treatment till the completion of treatment to see which is the fastest to achieve the end result

    Secondary Outcome Measures

    Full Information

    First Posted
    May 4, 2017
    Last Updated
    February 28, 2018
    Sponsor
    Guy's and St Thomas' NHS Foundation Trust
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03450551
    Brief Title
    Comparison of Efficacy of Three Orthodontic Appliances
    Official Title
    Comparison of Clinical Efficacy of Three Class II Correctors in Orthodontics, Prospective Expertise Matched Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 1, 2018 (Anticipated)
    Primary Completion Date
    August 2019 (Anticipated)
    Study Completion Date
    August 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Guy's and St Thomas' NHS Foundation Trust

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    To investigate each treatment modality in its "optimal" environment to avoid operator experience bias. Therefore we propose to operate out of three "specialist centres" with specific units providing one modality alone Which of the three orthodontic appliances does achieve best clinical progress, produce least discomfort to the patient, minimize the time taken for completion of treatment and maximize compliance.
    Detailed Description
    Patients and materials: The patient population will consist of patients age 10-16 that have, or are close to having, a full permanent dentition, and present to the clinic with Class II malocclusions with more than 1/2 unit II molar relationship. (Normal or deep overbite cases are also included). The treatments to be compared are the three (routinely-used) orthodontic appliances: Twin Block, Herbst and Frog. Hypothesis: The principal (null) hypothesis is that there is no difference between the three appliances in terms of their effectiveness, efficiency and compliance. Study design: The study is designed as a multicentre, Prospective Expertise Based Matched Controlled Longitudinal Trial and the assessments will be longitudinal in time. All patients that consent/assent to be part of the study (and their parents) will receive an information leaflet about the study and will be asked to sign an assent form. Patients are free to discontinue treatment if they wish to do so. The normal length of orthodontic treatment is between 18 and 24 months. Assessments will be taken prior to treatment and throughout the treatment period, with regular progress reviews every 3 months, as per standard practice. Outcomes: The principal outcome for efficiency is the time taken for completion of treatment. The principal outcomes for effectiveness are the clinical progress, discomfort (caused by the appliance to the patient) and compliance. Clinical progress will be assessed by measuring tooth movement on each review appointment, using radiographic examination (DPT and lateral cephalograms). Each patient will record discomfort in a visual analogue scale (VAS or Likert scale)and compliance by writing the days the appliance was not in the mouth for any reason. Covariates: Socio-economic variables: age, gender, etc.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    183 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Twin Block
    Arm Type
    Experimental
    Arm Description
    61 patients will receive the Twin Block appliance (one of the three appliances being studied)
    Arm Title
    Herbst
    Arm Type
    Active Comparator
    Arm Description
    61 patients will receive the Herbst appliance (one of the three appliances being studied)
    Arm Title
    Frog distalising appliance
    Arm Type
    Active Comparator
    Arm Description
    61 patients will receive the Frog distalising appliance (one of the three appliances being studied)
    Intervention Type
    Device
    Intervention Name(s)
    Twin Block, Herbst, Frog distalising appliance
    Intervention Description
    To study which of the three orthodontic appliances does achieve the best clinical progress, produce least discomfort to the patient, minimize the time taken for completion of treatment and maximize compliance.
    Primary Outcome Measure Information:
    Title
    Number of participants who have experienced discomfort related to wearing the appliance
    Description
    This is to check which appliance produces more discomfort compared to the other appliances using the Likert scale. Each question on the scale asks to rate the pain as either (no pain, slight pain, moderate pain, severe pain) or (strongly disagree, disagree, agree, strongly agree). Patients will choose a response which matches their experience.
    Time Frame
    18-24 months
    Title
    establishing which appliance has the fastest completion time
    Description
    The three appliances will be compared in 'months' from the start of treatment till the completion of treatment to see which is the fastest to achieve the end result
    Time Frame
    18-24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    10 Years
    Maximum Age & Unit of Time
    16 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients aged 10-16 years of age in the late mixed/permanent dentition with Class II malocclusions (Both Cl II div 1 and Cl II div 2) > 1/2 unit Class II molar relationship bilaterally (at least 3.5mm) Normal or deep overbite cases will be included Skeletal Class II relationship (ANB > 4°) Overjet ≥ 5 mm in Cl II/1 cases Non-extraction cases Exclusion Criteria: Children in the early mixed dentition Class I and Class III malocclusions Malocclusions with less than 1/2 unit II molar relationship Reduced overbite / anterior openbite Medically compromised patients, syndromic patients or patients with severe facial asymmetry Special needs patients not able to comply with instructions / difficulty with compliance Hypodontia or extracted permanent tooth (except third molars) Poor oral hygiene with both Gingival bleeding Index and Plaque Index scoring no more than 1
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Inas Nasr, Consultant
    Phone
    +447719595027
    Email
    inasnasr@hotmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Dirk Bister, Consultant
    Phone
    02071884415
    Email
    dirk.bister@kcl.ac.uk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Dirk Bister, Consultant
    Organizational Affiliation
    Guy's and St Thomas NHS Trust
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    No personal patient details will be shared. Only study data collected.

    Learn more about this trial

    Comparison of Efficacy of Three Orthodontic Appliances

    We'll reach out to this number within 24 hrs