Study to Compare Two Functional Appliances for Class II Malocclusions
Malocclusion, Angle Class II
About this trial
This is an interventional treatment trial for Malocclusion, Angle Class II focused on measuring Myofunctional appliance
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.
Sites / Locations
- Birmingham dental hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Twin Block
Button and Bead
Twin Block appliance
Button and Bead appliance