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Study to Compare Two Functional Appliances for Class II Malocclusions

Primary Purpose

Malocclusion, Angle Class II

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Button and Bead appliance
Twin Block appliance
Sponsored by
University of Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malocclusion, Angle Class II focused on measuring Myofunctional appliance

Eligibility Criteria

10 Years - 14 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • * Overjet ≥ 7mm

    • The normal overjet for a Caucasian population is in the range of 2-4mm. A functional appliance is used to allow for overjet reduction without extractions and/or to reduce the anchorage demands of the subsequent treatment with the Straight Wire Appliance (SWA). Clinically the overjet would need to be significantly increased for the treating clinician to consider the use of a functional appliance. Other similar studies have used an overjet of >6mm or ≥ 7mm. This study has elected for an initial overjet of ≥ 7mm to improve the studies external validity by making it more applicable to day-to-day clinical practice.
    • The initial overjet will be used to select patients. The majority of recent high level trials and systematic reviews that have provided a significant amount of the evidence base in the treatment of Class II malocclusions have defined subjects according to their initial overjet.

      * Age 10 to 14 years

    • This has been selected to match other studies relating to functional appliance treatment and reflect the most common clinical practice. The literature on functional appliance treatment has provided evidence that on average the enhancement of growth is small. Some studies on the timing of functional appliance treatment have suggested that pubertal growth is not a significant factor in the success of functional appliance treatment but it is well know and accepted that functional appliance treatment is assisted during periods of more rapid growth. Numerous studies have also found better co-operation and completion of treatment in younger patients (Banks 2004, KOB 2003a & 2003b)

      * Satisfactory Dental health

    • Patients must be dentally healthy and have a suitable level of oral health that would support orthodontic treatment, as per the British Orthodontic Society guidelines. They must have good oral hygiene with minimal gingivitis or periodontal disease, no dental caries or periapical pathology and no history of dento-alveolar trauma. This is judged by the investigator.

      • Willing to participate in study and provide informed consent

Exclusion Criteria:

  • * No previous orthodontic treatment or premolar extractions

    • This is aimed at reducing any confounding factors within the study as these may affect the success of treatment.

      * No craniofacial syndrome (including Cleft patients)

    • This is aimed at reducing any confounding factors within the study as these conditions may affect the success of treatment. The treatment of this subgroup requires a multi-disciplinary team and is more complex. Their treatment pathway may vary from normal clinical practice.

Sites / Locations

  • Birmingham dental hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Twin Block

Button and Bead

Arm Description

Twin Block appliance

Button and Bead appliance

Outcomes

Primary Outcome Measures

Change in overjet reduction
How quickly the horizontal discrepancy between upper and lower incisor edges is reduced

Secondary Outcome Measures

Change in Peer Assessment Rating (PAR)
PAR score change in terms of percentage and actual score
Drop out
Percentage of patients dropping out of each arm of the trial
Skeletal changes
Compare skeletal changes of landmarks in degrees and millimetres using cephalometric x-rays at various time points
3D soft tissue measures
Measure changes in soft tissues using 3D photographs
Patient satisfaction
Use of tailored patient satisfaction questionnaire to assess patient satisfaction with both appliances
Child related Oral health quality of life (OHRQoL) questionnaire
Changes in OHRQoL
Adverse events
Adverse events: decalcification, dental caries, soft tissue trauma, ingestion or aspiration of appliance

Full Information

First Posted
October 6, 2017
Last Updated
December 11, 2018
Sponsor
University of Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT03773783
Brief Title
Study to Compare Two Functional Appliances for Class II Malocclusions
Official Title
Effectiveness of Treatment for Class II Malocclusions With the Button & Bead or Twin-block Functional Appliance: A Single Centre Randomised Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Unknown status
Study Start Date
July 10, 2017 (Actual)
Primary Completion Date
July 2019 (Anticipated)
Study Completion Date
July 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Birmingham

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
A randomised controlled clinical trial to compare the effectiveness of two functional appliances in the correction of a Class II malocclusion. (Class II malocclusions are where upper front teeth bite significantly further forward in relation to lower front teeth). Null hypothesis: There is no significant difference between the Button & bead and Twin-block appliances with regard to time taken to reduce the overjet
Detailed Description
Background: A functional appliance is a type of brace used to help correct a 'Class II' malocclusion. Class II malocclusions are where upper front teeth bite significantly further forward in relation to lower front teeth. A functional appliance is defined as a brace that engages upper and lower teeth and works mainly by posturing the lower jaw away from its normal position1. The functional appliance may either be removable or fixed in nature and of various designs. Correction of a class II malocclusion can be commenced early i.e. before the age of 10 or during early adolescence when the patient is in a late mixed dentition / early permanent dentition. If correction is commenced early, this results in the need for a two phase treatment which involves functional appliance treatment in the first phase (age 7-10) followed by fixed appliances (+/- functional appliances) as an adolescent (age 11-16). If correction is started in early adolescence only one phase of treatment is required which involves a combination of functional and fixed appliances (age 11-16). Early or delayed class II treatment has been studied by various researchers2-10. O'Brien et al7 concluded that there was no advantage of early treatment with Twin Block as compared to treatment started in adolescents. In fact, they reported significantly poorer occlusal outcomes as determined by the objective Peer Assessment Rating (PAR) index in those that had early treatment. In addition, they found that total duration of treatment, total attendances and total cost of treatment was significantly higher in the early treatment group. The average total duration of treatment for those that had early treatment was 968 days (phase 1 = 527 days and phase 2 = 435 days) compared to 744 days for those that had treatment as an adolescent only. The most commonly used brace to correct class II malocclusions in the UK is a functional appliance (Twin Block design) 11. The Button and Bead functional appliance has been developed and used successfully by Mr Spary (Consultant Orthodontist) for several years. However, there are no studies to date that have studied its effectiveness in correcting a class II problem. The Button and bead appliance appears to be quicker at reducing the overjet and preferred by patients as there is less mouth opening making the appliance more comfortable to wear. It is also two clear aligners, which are more aesthetic than the traditional twin block appliance. The button and bead appliance does not however allow arch expansion. This may necessitate another appliance prior to fixed appliance treatment or prolong fixed appliance treatment if expansion also needs to be carried out in that phase. Objectives: Primary objective: a. To compare the Button-&-bead and Twin-block appliances treatment duration for overjet reduction Secondary objectives: To compare the Button-&-bead and Twin-block appliances dento-occlusal outcomes as measured by the Peer Assessment Rating (PAR) To compare patient compliance with the Button-&-bead and Twin-block appliances and identify causes for failure To compare the health economics of the Button-&-bead and Twin-block appliances (Cost of appliances, number of visits, number and cost of repairs and/or replacements) To compare the skeletal changes of the Button-&-bead and Twin-block appliances based on the Eastman analysis To compare changes in soft tissue profile as assessed by 3D photographs To assess changes in OHRQoL after overjet reduction with the Button-&-bead and Twin-block appliances To evaluate and compare patient satisfaction with the Button-&-bead and Twin-block appliances Safety objective To evaluate the safety of the Button-&-Bead appliance relative to the Twin-Block appliance in terms of the occurrence of any device-related adverse- and side-effects (soft-tissue trauma, decalcification, dental caries, ingestion or aspiration of appliance).

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Twin Block
Arm Type
Active Comparator
Arm Description
Twin Block appliance
Arm Title
Button and Bead
Arm Type
Experimental
Arm Description
Button and Bead appliance
Intervention Type
Device
Intervention Name(s)
Button and Bead appliance
Intervention Description
Button and Bead appliance
Intervention Type
Device
Intervention Name(s)
Twin Block appliance
Intervention Description
Twin Block appliance
Primary Outcome Measure Information:
Title
Change in overjet reduction
Description
How quickly the horizontal discrepancy between upper and lower incisor edges is reduced
Time Frame
Overjet measurement recorded at the start of treatment and at completion of functional appliance therapy 1 year later.
Secondary Outcome Measure Information:
Title
Change in Peer Assessment Rating (PAR)
Description
PAR score change in terms of percentage and actual score
Time Frame
PAR score will be Assessed from the start of treatment models and the end of fixed appliance study models ( 2 years later)
Title
Drop out
Description
Percentage of patients dropping out of each arm of the trial
Time Frame
No. of patients at the start of functional appliance therapy that do not wish to continue within the trial or do not finish functional appliance therapy within 18 months
Title
Skeletal changes
Description
Compare skeletal changes of landmarks in degrees and millimetres using cephalometric x-rays at various time points
Time Frame
Cephalometric x-rays at start of treatment and at the end of treatment 1 year later
Title
3D soft tissue measures
Description
Measure changes in soft tissues using 3D photographs
Time Frame
3D photographs at start of treatment and at the end of treatment (approx 1 year later)
Title
Patient satisfaction
Description
Use of tailored patient satisfaction questionnaire to assess patient satisfaction with both appliances
Time Frame
Patient satisfaction survey at study completion ( 1 year after treament started)
Title
Child related Oral health quality of life (OHRQoL) questionnaire
Description
Changes in OHRQoL
Time Frame
The patient ticked the applicable box for the 16 set questions from the standardised qualitative oral health questionairre. This was undertaken at the start of the trial and again at the end of functional appliance therapy ( approximately 1 year later)
Title
Adverse events
Description
Adverse events: decalcification, dental caries, soft tissue trauma, ingestion or aspiration of appliance
Time Frame
Adverse events over the course of functional appliance treatment ( recorded at every visit and reviewed at 1 year)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: * Overjet ≥ 7mm The normal overjet for a Caucasian population is in the range of 2-4mm. A functional appliance is used to allow for overjet reduction without extractions and/or to reduce the anchorage demands of the subsequent treatment with the Straight Wire Appliance (SWA). Clinically the overjet would need to be significantly increased for the treating clinician to consider the use of a functional appliance. Other similar studies have used an overjet of >6mm or ≥ 7mm. This study has elected for an initial overjet of ≥ 7mm to improve the studies external validity by making it more applicable to day-to-day clinical practice. The initial overjet will be used to select patients. The majority of recent high level trials and systematic reviews that have provided a significant amount of the evidence base in the treatment of Class II malocclusions have defined subjects according to their initial overjet. * Age 10 to 14 years This has been selected to match other studies relating to functional appliance treatment and reflect the most common clinical practice. The literature on functional appliance treatment has provided evidence that on average the enhancement of growth is small. Some studies on the timing of functional appliance treatment have suggested that pubertal growth is not a significant factor in the success of functional appliance treatment but it is well know and accepted that functional appliance treatment is assisted during periods of more rapid growth. Numerous studies have also found better co-operation and completion of treatment in younger patients (Banks 2004, KOB 2003a & 2003b) * Satisfactory Dental health Patients must be dentally healthy and have a suitable level of oral health that would support orthodontic treatment, as per the British Orthodontic Society guidelines. They must have good oral hygiene with minimal gingivitis or periodontal disease, no dental caries or periapical pathology and no history of dento-alveolar trauma. This is judged by the investigator. Willing to participate in study and provide informed consent Exclusion Criteria: * No previous orthodontic treatment or premolar extractions This is aimed at reducing any confounding factors within the study as these may affect the success of treatment. * No craniofacial syndrome (including Cleft patients) This is aimed at reducing any confounding factors within the study as these conditions may affect the success of treatment. The treatment of this subgroup requires a multi-disciplinary team and is more complex. Their treatment pathway may vary from normal clinical practice.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sheena Kotecha, FDS MPhil
Phone
(+44)07940544164
Email
drkotecha@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Dietrich
Email
T.Dietrich@bham.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Dietrich
Organizational Affiliation
University of Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Birmingham dental hospital
City
Birmingham
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sheena Kotecha

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Isaacson KG, Reed RT, Stephens CD. Functional orthodontic appliances. Oxford: Blackwell Scientific Publications; 1990.
Results Reference
background
PubMed Identifier
9457020
Citation
Tulloch JF, Phillips C, Proffit WR. Benefit of early Class II treatment: progress report of a two-phase randomized clinical trial. Am J Orthod Dentofacial Orthop. 1998 Jan;113(1):62-72, quiz 73-4. doi: 10.1016/S0889-5406(98)70277-X.
Results Reference
background
PubMed Identifier
9457018
Citation
Keeling SD, Wheeler TT, King GJ, Garvan CW, Cohen DA, Cabassa S, McGorray SP, Taylor MG. Anteroposterior skeletal and dental changes after early Class II treatment with bionators and headgear. Am J Orthod Dentofacial Orthop. 1998 Jan;113(1):40-50. doi: 10.1016/S0889-5406(98)70275-6.
Results Reference
background
PubMed Identifier
9457019
Citation
Ghafari J, Shofer FS, Jacobsson-Hunt U, Markowitz DL, Laster LL. Headgear versus function regulator in the early treatment of Class II, division 1 malocclusion: a randomized clinical trial. Am J Orthod Dentofacial Orthop. 1998 Jan;113(1):51-61. doi: 10.1016/s0889-5406(98)70276-8.
Results Reference
background
PubMed Identifier
12923506
Citation
O'Brien K, Wright J, Conboy F, Sanjie Y, Mandall N, Chadwick S, Connolly I, Cook P, Birnie D, Hammond M, Harradine N, Lewis D, McDade C, Mitchell L, Murray A, O'Neill J, Read M, Robinson S, Roberts-Harry D, Sandler J, Shaw I. Effectiveness of treatment for Class II malocclusion with the Herbst or twin-block appliances: a randomized, controlled trial. Am J Orthod Dentofacial Orthop. 2003 Aug;124(2):128-37. doi: 10.1016/s0889-5406(03)00345-7.
Results Reference
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PubMed Identifier
12970656
Citation
O'Brien K, Wright J, Conboy F, Sanjie Y, Mandall N, Chadwick S, Connolly I, Cook P, Birnie D, Hammond M, Harradine N, Lewis D, McDade C, Mitchell L, Murray A, O'Neill J, Read M, Robinson S, Roberts-Harry D, Sandler J, Shaw I. Effectiveness of early orthodontic treatment with the Twin-block appliance: a multicenter, randomized, controlled trial. Part 1: Dental and skeletal effects. Am J Orthod Dentofacial Orthop. 2003 Sep;124(3):234-43; quiz 339. doi: 10.1016/S0889540603003524.
Results Reference
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PubMed Identifier
19409339
Citation
O'Brien K, Wright J, Conboy F, Appelbe P, Davies L, Connolly I, Mitchell L, Littlewood S, Mandall N, Lewis D, Sandler J, Hammond M, Chadwick S, O'Neill J, McDade C, Oskouei M, Thiruvenkatachari B, Read M, Robinson S, Birnie D, Murray A, Shaw I, Harradine N, Worthington H. Early treatment for Class II Division 1 malocclusion with the Twin-block appliance: a multi-center, randomized, controlled trial. Am J Orthod Dentofacial Orthop. 2009 May;135(5):573-9. doi: 10.1016/j.ajodo.2007.10.042.
Results Reference
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PubMed Identifier
8338068
Citation
Nelson C, Harkness M, Herbison P. Mandibular changes during functional appliance treatment. Am J Orthod Dentofacial Orthop. 1993 Aug;104(2):153-61. doi: 10.1016/S0889-5406(05)81005-4.
Results Reference
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PubMed Identifier
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Citation
Illing HM, Morris DO, Lee RT. A prospective evaluation of Bass, Bionator and Twin Block appliances. Part I--The hard tissues. Eur J Orthod. 1998 Oct;20(5):501-16. doi: 10.1093/ejo/20.5.501.
Results Reference
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PubMed Identifier
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Citation
Thiruvenkatachari B, Sandler J, Murray A, Walsh T, O'Brien K. Comparison of Twin-block and Dynamax appliances for the treatment of Class II malocclusion in adolescents: a randomized controlled trial. Am J Orthod Dentofacial Orthop. 2010 Aug;138(2):144.e1-9; discussion 144-5. doi: 10.1016/j.ajodo.2010.01.025.
Results Reference
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PubMed Identifier
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Citation
Chadwick SM, Banks P, Wright JL. The use of myofunctional appliances in the UK: a survey of British orthodontists. Dent Update. 1998 Sep;25(7):302-8.
Results Reference
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Study to Compare Two Functional Appliances for Class II Malocclusions

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