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Malocclusion, Angle Class IINCT01530516

Crossbow Versus Forsus Springs in Mild to Moderate Class II Malocclusion Cases

A study testing Brackets plus Forsus springs and Xbow plus full brackets in people with Malocclusion, Angle Class II, run by University of Alberta at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Class II malocclusion (mismatch between the upper and lower jaw in which the lower jaw appears to be smaller from a profile point of view) are common in the general population. Around 1/3 of the population have some degree of this skeletal/dental problem and it is one frequent reason why patients decide to undergo… Read more about this study

Who is it for?
Ages 11 to 15 years
Conditions the study is for
Malocclusion, Angle Class II
What is being tested?
Brackets plus Forsus springs and Xbow plus full brackets
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 siteCanada
Study dates
1 Oct 2012to 31 Jul 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 11 to 15 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Participants will be of either gender between 11 and 15 years-of-age.
  • They will have mild to moderate Class II division 1 malocclusions.
  • Late mixed dentition or early permanent dentition.

Who cannot join

  • Severe vertical growth tendency or syndromic cases.
  • Craniofacial growth completed.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Edmonton Clinic

    Edmonton, Alberta, T6G 1C9

Other trials in Canada

About this study

Official title: 3D Changes Comparing the Crossbow Appliance and Later Full Fixed Brackets Against Simultaneous Use of Full Fixed Brackets Plus Forsus Springs Among Mild to Moderate Class II Malocclusion Cases: A Randomized Clinical Trial.

Class II malocclusion (mismatch between the upper and lower jaw in which the lower jaw appears to be smaller from a profile point of view) are common in the general population. Around 1/3 of the population have some degree of this skeletal/dental problem and it is one frequent reason why patients decide to undergo orthodontic treatment. Treatment alternatives will basically depend on the facial skeletal development of the patient and also on the magnitude of the skeletal/dental discrepancy.

For patients that are not yet fully skeletal mature, the treatment of mild to moderate Class II malocclusion involves a combination of a small skeletal growth modification effect and more significant dental movements. For skeletal mature individuals with a severe mismatch, the treatment usually involves jaw surgery to fully correct the malocclusion. For less severe cases orthodontic camouflage exclusively done by orthodontic movements is an option.

Read more

If the case is not severe enough to warrant a surgical approach there are several treatment alternatives. One of the most commonly used options is the use of orthodontic loaded springs that apply forces through brackets and arch wires bonded into the teeth so that the teeth will interrelate better.

A different alternative was proposed some years ago. The Xbow (spelled Crossbow) appliance differs from the above-proposed option in that no brackets are bonded or arch wires used. The orthodontic springs are applied to a metal framework cemented on some upper and lower teeth. Once the skeletal/dental problem is believed to have been significantly improved, fine tuning of the remaining dental problems is managed with brackets and arch wires. The theoretical advantage of such a design is that adverse effects, such as root resorption and decalcification from the long-term use of brackets and arch wires, are theoretically minimized as the brackets and arch wires have to be used for a shorter period of time.

Although there are some retrospective reports about the skeletal and dental effects of the Xbow appliance and only one prospective trial comparing the skeletal and dental changes to a non-treated growing sample; no randomized clinical trial has yet evaluated the changes compared to a current standard of care alternative which is the simultaneous use of loaded springs concurrent with brackets and arch wires.

Read the detailed description

Background

Class II malocclusion is a common orthodontic problem that requires comprehensive treatment planning. Treatment of Class II malocclusion is frequently initiated in mid to late mixed dentition whereby crowding and/or an increased over jet becomes alarming to patients and parents. Earlier correction of Class II abnormalities could be suggested in patients with significant occlusion discrepancies, increased risk of trauma to protruding upper incisors and impairment of mastication functions.

Among the available Class II correctors, cemented/fixed options are gaining popularity. Systematic reviews have shed some light on what fixed Class II correction devices appear to produce during treatment of mild to moderate Class II malocclusion. Short-term changes were a combination of skeletal and dental modifications. Skeletal modifications include both maxillary restriction and mandibular repositioning, and dental effects usually consist of inclination of mandibular incisors and maxillary molar distal movement.

Cephalometric analysis is a valuable tool used for diagnosis and treatment planning for dental malocclusion and underlying skeletal discrepancies. In view of the fact that a malocclusion is a product of an interaction between the alignment of the erupting teeth in their basal bone and the skeletal position of the basal bone itself, cephalometric analysis are used to evaluate dentoalveolar proportions and elucidate the anatomic basis for both jaw and tooth related abnormalities in the sagittal plane.

The Xbow appliance is a recently introduced orthodontic device that is used in late mixed or early permanent dentition before full fixed orthodontic treatment is initiated. Its main goal is to rapidly correct/improve the occlusion in a Class II malocclusion in mild to moderate cases. Full brackets thereafter will fine-tune the final occlusion.

Since its introduction there have been only three published studies of the Xbow appliance. One study focused on the evaluation of short-term skeletal and dental effects from lateral cephalograms while another discussed lower incisor inclination according to vertical facial types. Both reported mandibular incisor inclination of variable magnitude. The last published study analyzed if any conventionally utilized cephalometric variable was able to predict the amount of lower incisor inclination consistently.

As mentioned above, although the are some retrospective reports about the skeletal and dental effects of the Xbow appliance and only one pilot prospective trial comparing the skeletal and dental changes to a non-treated growing sample; no randomized clinical trial has yet evaluated the changes compared to a current standard of care alternative which is the simultaneous use of loaded springs concurrent with brackets and arch wires.

Objectives

The present study compares 3D facial, skeletal and dental changes using two orthopedic orthodontic approaches. Group 1 (alternative treatment) will use a fixed Class II corrector - Crossbow appliance - with full braces utilized later against Group 2 (one of the current available conventional treatments) with full fixed appliances with an additional fixed Class II corrector - (standard of care) - in clinical patients with mild to moderate Class II division 1 malocclusion.

An additional objective is to compare the adverse effects (root resorption and enamel decalcification) among both groups.

Methods

Each patient will undergo orthodontic clinical screening to determine if they fill the inclusion criteria (mild to moderate Class II malocclusion in a growing individual). Eligible candidates will be approached with an opportunity to participate in the research study. After understanding the research purpose and possible side effects, and they choose to participate, they will voluntarily sign the informed consent form. They will be randomly assigned to one of two groups. The researchers will not participate in the randomization as it would be done by a statistician and only communicated by phone once a participant is deemed to have fulfilled the inclusion criteria and provided informed consent.

Both treatment arms will start as soon as the randomization has been done. Full orthodontic records (digital volumetric images - Cone Beam Computer Tomograms, photos and dental casts) will be obtained for both groups at baseline and after treatment is completed.

Group 1 treatment will consist of fixed orthodontic appliances (brackets and molar tubes) with the addition of the spring loaded orthodontic corrector once occlusion level and alignment has been completed as per standard of care. It is expected that the treatment will last around 24 months.

Group 2 treatment will consist of a fixed functional Crossbow appliance. Bands will be fitted in the lower first molars, as well as in the upper first molars. A lingual and a vestibular arch connecting the lower molar bands, as well as a Hyrax type rapid maxillary expansion connecting the upper bands will be made in the laboratory. A Forsus spring will be connected from a molar tube in the upper first molar to lower vestibular arch with adjustable Guerin locks. It is expected that the Xbow treatment will be around 6 to 8 months. Fixed orthodontic appliances (brackets and molar tubes) will be inserted thereafter and the regular orthodontic treatment will be provided with an expected additional completion time of 12 to 16 months. Therefore total treatment time will be in the 24-month range.

A sample of 50 patients (25 patients per treatment group, considering a 20% loss during follow-up so that the groups will not have less than 21 patients per group at the end of study) will be sought. Assumptions made were with a SD of 5 degrees of lower incisor inclination, as averaged from previous studies, and a clinically significant difference of also 5 degrees.

Being tested
Brackets plus Forsus springs, Xbow plus full brackets
Keywords
Malocclusion, Angle Class II
Medical subject headings
Malocclusion, Angle Class II

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Brackets plus Forsus springsDevice

    Also called Forsus™ Fatigue Resistant Device

    Full brackets and after completion of level and alignment insertion of Class II correctors (Forsus spring devices).

  • Xbow plus full bracketsDevice

    Also called Xbow Class II corrector

    Xbow appliance to be inserted first. After anteroposterior changes have been completed full brackets will be bonded and occlusion fine tuned

Study groups in NCT01530516
Study groupRoleWhat they receive
Full brackets plus Forsus springsActive comparatorStandard of care - Class II springs used after le el and alignment.
Receives: Device: Brackets plus Forsus springs
Xbow plus full bracketsExperimentalAlternative treatment - First use the Xbow appliance and then full brackets after Class II occlusion has been corrected.
Receives: Device: Xbow plus full brackets

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Facial soft tissue, dental and skeletal changes

    Outcomes to be measured from Computer Beam Computer Tomography data and dental casts.

    Measured: 24 months

Secondary outcomes (2)
  1. Root resorption

    Evaluation of the magnitude of external root resorption as quantified/qualified from the CBCT data.

    Measured: 24 months

  2. Enamel decalcification

    Enamel decalcification as clinically determined by observing and touching the enamel surfaces of teeth.

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Feb 2012 (estimated)
  2. Study start1 Oct 2012
  3. Primary completion31 Jul 2018
  4. Study completion31 Jul 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01530516
Sponsor's protocol ID
Pro00021423
Status last verified
Nov 2024
First submitted
7 Feb 2012
Last updated
5 Nov 2024
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Brackets plus Forsus springs and Xbow plus full brackets in people with Malocclusion, Angle Class II, run by University of Alberta at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Facial soft tissue, dental and skeletal changes (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Nov 2024.

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