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Malocclusion, Angle Class IINCT02456220

Dentoskeletal Changes Associated With Herbst Appliance Therapy

A study testing Herbst appliance in people with Malocclusion, Angle Class II, run by Bernardo Quiroga Souki at 1 site in Brazil.

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

The aim of the study is to perform a three-dimensional (3D) evaluation of the dentoskeletal changes in pubertal Class II malocclusion subjects treated with the Herbst appliance (HAG), in comparison with a Class II comparison group (CG). Read more about this study

Who is it for?
Ages 12 to 16 years
Conditions the study is for
Malocclusion, Angle Class II
What is being tested?
Herbst appliance
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteBrazil
Study dates
Mar 2013to Oct 2015
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 12 to 16 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Class II malocclusion with mandibular retrognathism
  • Convex Profile
  • Pubertal period
  • Permanent dentition
  • Parental permission with a signed consent form

Who cannot join

  • Syndromic patients
  • Previous orthopedic treatment

Trial locations and contacts

1 site in 1 country.

Brazil1 site
  • Pontifícia Universidade Católica de Minas Gerais

    Belo Horizonte, Minas Gerais, 30.535.610

Other trials in Brazil

About this study

Official title: Three-dimensional Assessment of the Dentoskeletal Changes Associated With Herbst Appliance Therapy: A Controlled Clinical Trial

The aim of the study is to perform a three-dimensional (3D) evaluation of the dentoskeletal changes in pubertal Class II malocclusion subjects treated with the Herbst appliance (HAG), in comparison with a Class II comparison group (CG). 3D virtual models generated from three time-point CBCTs (T0, baseline; T1, immediately after Herbst insertion; and T2, 8 months after) of 25 HAG patients will be evaluated. Virtual models obtained from 25 Class II malocclusion patients, in the same stage of biologic maturation and skeletal abnormality, but with no orthopedic treatment will be constructed for the CG subjects. These CG patients are under orthodontic treatment, but only with teeth alignment. Voxel based registration on the anterior cranial fossa will be used to assess maxillary and mandibular displacement/articular fossa remodeling; regional registration on the mandibular corpus will be performed to evaluate mandibular growth and mandibular dental changes; and regional registration on the anterior region of the maxilla will be performed to evaluate maxillary growth and maxillary dental changes.

Read the detailed description
  1. BACKGROUND Class II malocclusion is highly prevalent worldwide, and it is a major reason for orthodontic treatment to be initiated. This type of malocclusion can be restricted to the dentoalveolar region, but the majority of Class II patients exhibit a strong skeletal component to the malocclusion, including most frequently mandibular skeletal retrusion and an increased lower anterior facial height. With increased severity of the mandibular deficiency, the orthodontist is challenged to treat the underlying skeletal problem appropriately. For growing patients, the use of fixed and removable mandibular advancement appliances has been advocated for many decades. A variety of fixed Herbst appliance designs have achieved worldwide acceptance in that they eliminate most major patient compliance factors. Today the Herbst appliance (HA) is by far the most frequently used mandibular jumping device in the United States, with more Herbst appliance being fabricated than all other functions appliances combined. The Herbst appliance originally was introduced by Emil Herbst in the early years of the twentieth century, but it did not achieved worldwide clinical acceptance until its re-introduction by Hans Pancherz 70 years later. Since then, a significant number of clinical and scientific studies has been conducted about HA, particularly by Pancherz and colleagues. Two-dimensional cephalometric studies have reported increases in the length of the mandible and in forward displacement of the mandible following HA in comparison to matched untreated controls. On average, 2 mm of mandibular length gain (measured from Gonion to Pogonion) and 1.5 degree of improvement in the SNB angle can be observed following Herbst appliance therapy. Investigations in experimental animals have provided the histological evidence of the changes in the condyles, rami, and articular fossae when the mandible is advanced in a laboratory setting. Previous reports have showed an increased proliferation of the condylar cartilage in monkeys that had their mandible advanced with the Herbst appliance. These adaptations occurred primarily in the posterior and posterosuperior regions of the condyle. They also reported significant bone deposition along the posterior border of the mandibular ramus during the early part of the experimental period as well as significant deposition of new bone on the anterior surface of the postglenoid spine at the articular fossae. It should be noted, however, that the post-glenoid spine is not well-defined in humans. Clinical investigations using Magnetic Ressonance Imaging (MRI) and lateral radiographs have showed that changes in the mandibular condyles and articular fossae may occur with Herbst therapy. It has been demonstrated that following Herbst therapy some articular fossa remodeling can be seen at the anterior surface of the postglenoid spine, which causes a relocation of the articular fossae in a downward and forward direction. But such fossa adaptation in Herbst patients is less extensive than in experimental animals, with much individual variation in response evident. Although most Herbst studies are convergent as to the extent of skeletal and dentoalveolar adaptations, some questions still remain:
  • How much mandibular growth can be achieved with therapeutic mandibular advancement?
  • How much mandibular rotation and skeletal bite opening occurs?
  • How much of the original mandibular advancement is maintained long-term?
  • Is there is an adaptive behavior of the articular fossa after mandibular advancement, with bone remodeling occurring in the fossa. In the last decade, a new methodology using 3D virtual modeling has been developed allowing a change in the paradigm of assessing the skeletal changes associated with growth and treatment; this technology that has opened new horizons in scientific investigations of dentofacial orthopedics. Recently, the American Journal of Orthodontists and Dentofacial Orthopedics published the first 3D report on Herbst treatment, a pilot study in which 7 Class II subjects treated with the Herbst appliance were compared with 7 Class II subjects treated with fixed appliances and intermaxillary elastics. It was reported that Class II patients undergoing Herbst treatment demonstrated anterior displacement of the condyles and articular fossae along with maxillary restraint when compared with the Class II patients used for comparison. The aim of the present prospective controlled clinical trial is to investigate the skeletal changes in the mandible and articular fossae in Class II patients undergoing Herbst appliance therapy, using 3D virtual models in comparison to a control group comprising Class II subjects.
  1. PATIENTS AND METHODS b.1) Study design

This is a non-randomised controlled clinical trial, with intervention. Two groups are been planned: 1) Class II malocclusion subjects treated with Herbst appliance (HAG); and 2) Class II malocclusion subjects treated only with teeth alignment. The two groups are matched by stage of skeletal maturation, type of malocclusion, chronological age, and gender. There is no blinding for the outcome evaluators. Due to ethical concerns, the comparison group will be composed of Class II subjects that need previous alignment and leveling of the teeth before orthopedic phase of their treatment.

b.2) Participants - settings and location where the data are collected The treatment are been performed in the Orthodontic Clinic of Pontifical Catholic University of Minas Gerais (Belo Horizonte, Brazil). This is a private university, but the patients are mostly low-income subjects. Data has been collected from August 2013 and finished on September 2015.

b3) Sample size Based on the standard deviation of 1.85 mm reported by Pancherz et al.28, an alpha significance level of 0.05 and a power of 0.80 to detect changes of 1.5 mm, a preliminary sample size of 25 patients per group was calculated.

Therefore, 25 individuals have received a Herbst appliance at the beginning of their treatment with a one-step full activation - Herbst Appliance Group (HAG); while 25 skeletal Class II malocclusion individuals, with indication for HA therapy, but with other clinical conditions that required prior treatment before HA insertion, have been allocated to the CG. The two groups have been matched by chronological age (between 12 years and 16 years-old), by stage of skeletal maturation and by the stage of dental development (permanent dentition).

b4) Appliance design

The Herbst appliance design included bilateral telescoping arms (3M Abzil, São José do Rio Preto, Brazil) articulated with pivots that were positioned in both the maxillary and mandibular arches. The pivots were welded to a rigid cantilever wire (.040-in stainless steel) extending from the lower first permanent molar bands (TP Orthodontics, La Porte, IN) to the canine regions of the mandible. In the maxillary arch, the pivots were welded to bands on the permanent first molars. A Hyrax expander (Morelli Ortodontia, Sorocaba, Brazil) and a .040-in stainless steel (SS) lower lingual arch were added to the HA structure to improve appliance stability and transverse dimensional control. Two .028-in SS wires were used as occlusal rests in the permanent second molars to avoid their extrusion after activation. The occlusal rests were removed when they interfered with the occlusion to avoid bite opening.

b5) Method of registration

Cone beam computed tomography (CBCT), intra-oral pictures, and extra-oral pictures have been collected in three time-points for HAG (T0, T1, and T2), and in two time-point for CG (T0, and T2), as a regular protocol of orthodontic record for these clinical treatments.

b6) Method of measurement

Analysis of serial CBCT images to evaluate changes between T0, T1, and T2 include 3D analysis methodology using ITK-SNAP (open-source software, www.itksnap.org); SLICER (open-source software, www.slicer.org; and VAM - Vectra Analysis Model software version 3.7.6 (Canfield Scientific Inc., Fairfield, NJ). The tridimensional image analysis procedures included: (1) approximation of scans; (2) construction of 3D label models; (3) voxel based image registration; and (4) quantitative and qualitative assessments using 3D mesh surface models.

Quantitative assessment of the positional changes between the 3D surface models of the cranial base, maxilla, and mandible will be performed using point-to-point landmarks measurements (VAM software), and virtual analytics (SLICER software).

Interactive visual analytics include graphic displays with qualitative assessments using semitransparent overlays of the 3D surface models at the different time-points and quantitative assessments of the surface displacements using color-coded surface distance maps. All visual analytics assessments will be performed using two modules (Model-to-Model Distance and Shape Population Viewer) in the SLICER software.

Voxel based registration on the anterior cranial fossae will be used to assess maxillary and mandibular displacement/articular fossae remodeling; regional registration on the mandibular symphysis will be performed to evaluate mandibular growth and mandibular dental changes; and regional registration on the anterior region of the maxilla will be performed to evaluate maxillary growth and maxillary dental changes.

b7) Method of analysis

For the primary and secondary outcome measures it will be used Statistical Package for the Social Science (SPSS) software (version 16.0 Chicago, IL). Descriptive statistics will be presented for both groups. Statistical differences between the two groups will be calculated with Mann-Whitney test (comparison between the difference of the means of the HAG and CG). The comparison between the changes within each group will be performed using the Wilcoxon's test.

Being tested
Herbst appliance
Keywords
Herbst appliance, Computed tomography, 3D imaging, Growth and development, Orthodontic Appliances, Functional
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.

  • Herbst applianceDevice

    Group treated with conventional Herbst appliance for mandibular advancement during orthopedic treatment.

Study groups in NCT02456220
Study groupRoleWhat they receive
Herbst GroupExperimentalPatients treated with Herbst appliance.
Receives: Device: Herbst appliance
Comparison GroupNo interventionPatients that received only teeth movement (alignment and leveling before Herbst insertion), without any orthopedic intervention.

What is being measured

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

  1. Skeletal mandibular growth after Herbst appliance therapy

    To test the mandibular rotation immediately after Herbst appliance insertion; and 2) to compare the displacement of the condyles with the reduction of overjet (OJ) and overbite (OB). Virtual 3D surface models of 25 subjects were generated from the cone-beam computed tomographs taken before treatment, and immediately after Herbst installation. Scans were registered on the cranial bases, and analyzed using point-to-point measurements, color-coded maps and semitransparent overlays.

    Measured: 8 months

Secondary outcomes (5)
  1. Mandibular displacement after Herbst appliance therapy

    Based on cranial base volumetric superimposition, the assessment of the mandibular displacement will be performed. Based on regional superimposition of the mandibular corpus, the condilar and ramus growth will be evaluated.

    Measured: 8 months

  2. Displacement of the mandibular condyles immediately after Herbst appliance insertion - 3D assessment

    To test the mandibular rotation immediately after Herbst appliance insertion; and 2) to compare the displacement of the condyles with the reduction of overjet (OJ) and overbite (OB). Virtual 3D surface models of 25 subjects were generated from the cone-beam computed tomographs taken before treatment, and immediately after Herbst installation. Scans were registered on the cranial bases, and analyzed using point-to-point measurements, color-coded maps and semitransparent overlays.Scans were registered on the cranial bases, and analyzed using point-to-point measurements, color-coded maps and semitransparent overlays.

    Measured: 5 weeks

  3. Maxillary displacement after Herbst appliance therapy

    Evaluation of the maxillary displacement at the end of the treatment with the reference of the cranial base.

    Measured: 8 months

  4. Bone remodeling of the articular fossae after Herbst appliance therapy

    Evaluation of the bone remodeling of the articular fossae at the end of the treatment with the reference of the cranial base.

    Measured: 8 months

  5. Dental positional changes after Herbst appliance therapy

    Evaluation of the teeth movement at the end of the treatment with the reference of the maxilla and the mandible.

    Measured: 8 months

Timeline

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

  1. First posted28 May 2015 (estimated)
  2. Study startMar 2013
  3. Primary completionSep 2015
  4. Study completionOct 2015

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
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02456220
Sponsor's protocol ID
PUCMinasGerais
Status last verified
Oct 2015
First submitted
25 May 2015
Last updated
27 Oct 2015
Results posted
No
Data monitoring committee
No

Publications

  • Buschang PH, Tanguay R, Demirjian A, LaPalme L, Turkewicz J. Mathematical models of longitudinal mandibular growth for children with normal and untreated Class II, division 1 malocclusion. Eur J Orthod. 1988 Aug;10(3):227-34. doi: 10.1093/ejo/10.3.227. No abstract available.

    PubMed 3181302
  • Buschang PH, Martins J. Childhood and adolescent changes of skeletal relationships. Angle Orthod. 1998 Jun;68(3):199-206; discussion 207-8. doi: 10.1043/0003-3219(1998)0682.3.CO;2.

    PubMed 9622756
  • Cevidanes LH, Oliveira AE, Grauer D, Styner M, Proffit WR. Clinical application of 3D imaging for assessment of treatment outcomes. Semin Orthod. 2011 Mar 1;17(1):72-80. doi: 10.1053/j.sodo.2010.08.012.

    PubMed 21516170
  • Cevidanes LH, Heymann G, Cornelis MA, DeClerck HJ, Tulloch JF. Superimposition of 3-dimensional cone-beam computed tomography models of growing patients. Am J Orthod Dentofacial Orthop. 2009 Jul;136(1):94-9. doi: 10.1016/j.ajodo.2009.01.018.

    PubMed 19577154
  • Hagg U, Rabie AB, Bendeus M, Wong RW, Wey MC, Du X, Peng J. Condylar growth and mandibular positioning with stepwise vs maximum advancement. Am J Orthod Dentofacial Orthop. 2008 Oct;134(4):525-36. doi: 10.1016/j.ajodo.2006.09.064.

    PubMed 18929270
  • Hagg U, Pancherz H. Dentofacial orthopaedics in relation to chronological age, growth period and skeletal development. An analysis of 72 male patients with Class II division 1 malocclusion treated with the Herbst appliance. Eur J Orthod. 1988 Aug;10(3):169-76. doi: 10.1093/ejo/10.3.169. No abstract available.

    PubMed 3181295
  • Kinzinger G, Kober C, Diedrich P. Topography and morphology of the mandibular condyle during fixed functional orthopedic treatment --a magnetic resonance imaging study. J Orofac Orthop. 2007 Mar;68(2):124-47. doi: 10.1007/s00056-007-0650-0. English, German.

    PubMed 17372710
  • LeCornu M, Cevidanes LH, Zhu H, Wu CD, Larson B, Nguyen T. Three-dimensional treatment outcomes in Class II patients treated with the Herbst appliance: a pilot study. Am J Orthod Dentofacial Orthop. 2013 Dec;144(6):818-30. doi: 10.1016/j.ajodo.2013.07.014.

    PubMed 24286905
  • Pancherz H, Malmgren O, Hagg U, Omblus J, Hansen K. Class II correction in Herbst and Bass therapy. Eur J Orthod. 1989 Feb;11(1):17-30. doi: 10.1093/oxfordjournals.ejo.a035960.

    PubMed 2714389
  • Pancherz H. The effect of continuous bite jumping on the dentofacial complex: a follow-up study after Herbst appliance treatment of class II malocclusions. Eur J Orthod. 1981;3(1):49-60. doi: 10.1093/ejo/3.1.49. No abstract available.

    PubMed 6939593
  • Pancherz H. The mechanism of Class II correction in Herbst appliance treatment. A cephalometric investigation. Am J Orthod. 1982 Aug;82(2):104-13. doi: 10.1016/0002-9416(82)90489-4.

    PubMed 6961781
  • Pancherz H. Vertical dentofacial changes during Herbst appliance treatment. A cephalometric investigation. Swed Dent J Suppl. 1982;15:189-96.

    PubMed 6963773
  • Pancherz H. The Herbst appliance--its biologic effects and clinical use. Am J Orthod. 1985 Jan;87(1):1-20. doi: 10.1016/0002-9416(85)90169-1.

    PubMed 3855346
  • Pancherz H. The nature of Class II relapse after Herbst appliance treatment: a cephalometric long-term investigation. Am J Orthod Dentofacial Orthop. 1991 Sep;100(3):220-33. doi: 10.1016/0889-5406(91)70059-6.

    PubMed 1877546
  • Pancherz H, Anehus-Pancherz M. Muscle activity in class II, division 1 malocclusions treated by bite jumping with the Herbst appliance. An electromyographic study. Am J Orthod. 1980 Sep;78(3):321-9. doi: 10.1016/0002-9416(80)90277-8. No abstract available.

    PubMed 6931496

Questions about this trial

What is this clinical trial studying?

A study testing Herbst appliance in people with Malocclusion, Angle Class II, run by Bernardo Quiroga Souki at 1 site in Brazil.

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 5 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 27 Oct 2015. 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 Brazil. 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?

Skeletal mandibular growth after Herbst appliance therapy (time frame: 8 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02456220, which also lists 30 linked publications.

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 27 Oct 2015.

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