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
About this trial
This is an interventional treatment trial for Malocclusion, Angle Class II
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
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
NCT ID
NCT03450551
First Posted
May 4, 2017
Last Updated
February 28, 2018
Sponsor
Guy's and St Thomas' NHS Foundation Trust
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
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