Effects of the Herbst Appliance With Different Anchorages and Twin-Block Appliance in Class II Malocclusion (HASA)

October 24, 2022 updated by: Klaus Barretto-Lopes

Effects of the Herbst Appliance With Skeletal Anchorage or Dental Anchorage, and Twin-Block Appliance in Class II Malocclusion: A Randomized Clinical Trial

The purpose of this study is to determine if the Herbst appliance with indirect skeletal anchorage in mini-implants is capable of preventing excessive inclination of the lower incisors at the end of the treatment when compared to the Herbst appliance with dental anchorage and Twin-Block appliances in patients with Class II malocclusion and overjet ≥ 6 mm.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

2a. Background

The prevalence of the Angle Class II malocclusion is high, comprising almost half of known orthodontic problems (Silva Filho et al., 1990; Proffit et al., 1998). The Class II malocclusion is frequently responsible for negative aesthetic of the facial profile. This can result in psychosocial problems, principally in the Angle Class II, division I malocclusion because of the pronounced projection of the anterior superior teeth. This projection has also been related to fracture and avulsion of the anterior superior teeth.

Different types of appliances had been developed for the treatment of the Angle Class II malocclusion. Among these, functional orthopedic appliances have been used because they can correct Class II malocclusion with better improvement in the growth of the mandible when compared to headgears, which also can correct the problem, but with better restriction of the growth of the maxilla (Tulloch et al., 1997).

The Herbst appliance is a fixed functional orthopedic appliance that is often used because of its non-compliance-nature and the positive results achieved. Emil Herbst created the Herbst appliance in the 1910s (Pancherz; Ruf, 2008), but it was forgotten for decades. Only in the 1970s, Pancherz began a study of the Herbst appliance, and reported the positive results obtained in treatment of the Class II, division I malocclusion (Pancherz, 1979). Several subsequent studies of the Herbst appliance provided new scientific evidence of its benefits.

Nowadays, the Herbst appliance is often used in the treatment of Class II malocclusions, because of its efficiency (Bremen, Pancherz, 2008) and also because of the positive effects in orthodontic and orthopedic correction (Franchi et al., 1999). However, some investigators have stated that the correction of a Class II malocclusion is a result of anchorage loss, and could be responsible for negative effects on the lower incisors such as protrusion and gingival recession (Pancherz, 1979; Pancherz; Hansen, 1986; Pancherz; Hansen, 1988; Schütz et al., 2002; Vigorito; Yared et al., 2006; Dominguez, 2007).

Some attempts have been made to reduce the negative effects on lower incisors caused by the Herbst appliance, such as increasing the number of teeth in the mandibular anchorage, using soft-tissue anchorage, splints, and cast splints anchorage (Weschler et al., 2005; El-Fateh et al., 2011). However, these attempts were unsuccessful.

With the intention of solving these problems, a mini-implant prototype was developed for Herbst appliance anchorage (Barretto-Lopes, 2004). Mini-implants and implants have been used as anchors in orthodontics, for different purposes in different locations (Kanomi, 1997; Deguchi et al., 2003; Miyawaki et al., 2003). Some investigators have suggested the use of mini-implants as orthopedic anchors in animals (Smalley et al., 1988; De Pauw et al., 1999) and in the treatment of Class III malocclusions with retrusive maxillae in humans (Enacar et al., 2003, DeClerck et al., 2010; Heyman et al., 2010). However, there is little information about the use of mini-implants as an orthopedic anchor in the treatment of Class II malocclusions.

Therefore, a first in vitro study was developed to test the flexural resistance of the mini-implant prototypes developed for Herbst appliance anchorage (Barretto-Lopes, 2010, 2010). Subsequently, a question arose with respect to the resistance strength of these mini-implant prototypes when inserted in the bone, and a second ex vivo study was designed to evaluate if the mini-implant prototypes were capable of withstanding orthopedic forces in Minipigs br 1, and to compare the prototype resistance between the sites of insertion. The results showed that the mini-implant prototypes inserted in bone were capable of withstanding orthopedic forces (20.55 kgf for the mandible and 13.86 kgf for the maxilla), and the anterior region of the mandible could withstand statistically significant higher forces than the posterior region of the maxilla (Barretto-Lopes et al., 2012).

The next step was to test the Herbst with skeletal anchorage in humans and a pilot study was performed in patients to test the Herbst appliance with direct anchorage in mini-implants. However, the mini-implants presented mobility in the three cases tested and the trial was suspended.

Probably the direct load in mini-implants would be the reason of the system failure and a second pilot study in humans was carried out using the Herbst appliance with indirect anchorage in mini-implants. This system proved to be stable.

Thus, an in vivo study is necessary to evaluate the effect of the Herbst appliance with indirect anchorage in mini-implants on the lower incisors at the end of treatment compared to the Herbst appliance with dentoalveolar anchorage. Secondarily, this study could evaluate other dental effects and skeletal effects in the maxilla and mandible, resulting from the use of two types of anchoring.

2b. Objectives

Primary objective To determine if the Herbst appliance with indirect skeletal anchorage in mini-implants is capable of preventing excessive inclination of the lower incisors at the end of the treatment when compared to Herbst appliance with dental anchorage and Twin-Block appliances in patients with Class II malocclusion.

Secondary objectives To evaluate the changes occurred on mandible, maxilla, relationship between maxilla and mandible, lower molar and upper molar at the end of the treatment with the Herbst appliance with skeletal and dental anchorage, and Twin-Block appliances in patients with Class II malocclusion.

3-12. Methods

3a. Study design

According to the norms of the CONSORT STATEMENT (Moher et al., 2010), this study will be clinical with intervention, in which the allocation of the subjects will be randomized (block randomization). This study will be parallel, stratified by gender, with blinding for the outcome evaluators. The primary purpose of this study will be treatment.

4b. Participants - Settings and locations where the data are collected

The treatment will be performed in the Orthodontics Clinic of Rio de Janeiro State University. This public university serves a predominantly low-income population located in the Vila Isabel neighborhood in northern Rio de Janeiro State, Brazil. The estimated population size is 81,858 habitants (IBGE - CENSO 2000). Data will be collected from April 2015 through August 2016.

5. Interventions

Three groups will receive treatment. Group 1 will be treated with the Herbst appliance with dental anchorage for 12 months. Group 2 will be treated with the Herbst appliance with skeletal anchorage in mini-implants for 12 months. Group 3 will be treated with Twin-Block appliances.

7a. Sample size

The open source software developed by Harvard University (http://hedwig.mgh.harvard.edu/sample_size/js/js_parallel_quant.html) was used for the sample size calculation. The main outcome measure was the difference between lower incisor proclination before and after treatment. Standard deviation of 1.31 (Martin, Pancherz, 2009) with a two-tailed curve was considered. Difference in means of 2 mm was used as minimal detectable difference. This value was based on a question answered by Professors and Post graduation students who reported a reduction of 2 mm as clinically significant. The significance level will be ≤ 5% and the power of the study will be 80%.

Therefore, 57 subjects will be needed, with 19 subjects in each group. An Intention-to-treat analysis will be performed to deal with dropouts and multiple imputation will be used to deal with missing data. The treatment time will be, approximately, 12 months.

7b. Interim analysis and stopping guidelines

In the group with indirect skeletal anchorage, in case of mobility in the mini-implants in any subject, the load will be removed for about one month. After that, the load will be restored. If the mobility persists, the mini-implant will be removed and reinserted in another site. If mobility occurs again, this subject will be reallocated to the group with dental anchorage. The same procedure will be followed in case of failure of the mini-implant.

8. Randomization

8a. Sequence generation

The randomization of the clinical research will be done with a randomized list, using the first generator from the site www.randomization.com (Pandis et al., 2011).

8b. Type

The type of randomization will be block randomization. In this approach, after the selection of the subjects according to the eligibility criteria, the sample will be separated into 10 blocks with 6 subjects in each.

9. Allocation and concealment mechanism

The sequence of allocation will be concealed in sequential opaque envelopes numbered from 1 to 60, with the treatment modality.

10. Implementation

Before the beginning of the research, the secretary of the Department of Orthodontics of the Faculty of Dentistry of the University of the State of Rio de Janeiro will be responsible for the implementation of the randomization (generation and storage of the randomized list, allocation concealment and treatment assignment). The subjects will write their names on the numbered envelopes, and will open the envelopes to learn the treatment for which they were selected. After that, the envelopes will be closed with the type of treatment selected for storage of the information.

11. Blinding

Blinding will be carried out only for the data analysis because the researchers, participants and subjects will know the treatment modality. Therefore, a person who does not know in which group a subject was treated will analyze the data.

12. Statistical methods

For the primary and secondary outcome measures, the data analysis will be performed using SPSS statistical software package (version 12.0, Chicago). Means, standard deviations, and ranges of the dental and skeletal measures will be calculated for the Herbst appliance with dental anchorage and for the Herbst appliance with indirect skeletal anchorage. Statistical differences will be assessed using analysis of variance. The Wilcoxon's test will be used to assess dental and skeletal differences between the Herbst with dental anchorage and Herbst with indirect skeletal anchorage. Measurements will be repeated after 1 week by an examiner, and intraexaminer correlation coefficients (ICC) will be used to evaluate the reliability of repeated measures. A 1-sample test will be performed on duplicate measurements to test for systematic errors.

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Brazil
      • Rio de Janeiro, Brazil, 20551-030
        • Recruiting
        • Rio de Janeiro State University
        • Contact:
        • Contact:
        • Principal Investigator:
          • Klaus B Lopes, PhD
        • Sub-Investigator:
          • Jose Augusto M Miguel, PhD
        • Sub-Investigator:
          • Cátia C Quintão, PhD
        • Principal Investigator:
          • Tatiana A Lima, PhD
        • Sub-Investigator:
          • Nathalia Palomares, MSc

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years to 14 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Teenagers aged from 10 to 14 years old (both genders)
  • Parental permission with a signed consent form
  • Referral from the Orthodontics Clinic of the State of Rio de Janeiro University or private clinics
  • Presenting Class II, Division 1 malocclusion with convex profile and minimum overjet of 6 mm in permanent dentition.

Exclusion Criteria:

  • Missing teeth.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Herbst appliance with skeletal anchorage
Group treated with the Herbst appliance with indirect skeletal anchorage in mini-implants.
Device: Herbst appliance with skeletal anchorage
Group treated with the Herbst appliance with indirect skeletal anchorage in mini-implants.
Active Comparator: Herbst appliance with dental anchorage
Group treated with the conventional Herbst appliance with dental anchorage.
Device: Herbst appliance with dental anchorage
Group treated with the conventional Herbst appliance with dental anchorage.
Active Comparator: Twin-Block appliances
Group treated with Twin-Block appliance.
Device: Twin-Block appliance
Group treated with Twin-Block appliance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lower incisors position changes as measured by tomographic superimposition of the mandible.
Time Frame: 12 months
Comparison in lower incisors position between the two groups at the end of the treatment.
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morphological mandible changes as measured by tomographic superimposition of the cranial base.
Time Frame: 12 months
Comparison between the changes of the mandible in the two groups at the end of the treatment.
12 months
Maxilla changes as measured by tomographic superimposition of the cranial base.
Time Frame: 12 months
Comparison between the changes of the maxilla in the two groups at the end of the treatment.
12 months
Changes in relationship between maxilla and mandible as measured by tomographic superimposition of the cranial base.
Time Frame: 12 months
Comparison between the changes of the relationship between the maxilla and the mandible in the two groups at the end of the treatment.
12 months
Lower molar position changes as measured by tomographic superimposition of the mandible.
Time Frame: 12 months
Comparison between the changes of the lower molar in the three groups at the end of the treatment.
12 months
Upper molar position changes as measured by tomographic superimposition of the maxilla.
Time Frame: 12 months
Comparison between the changes of the upper molar in the three groups at the end of the treatment.
12 months
Facial changes as measured by tomographic superimposition of the face
Time Frame: 12 months
Comparison between the facial changes in the three groups.
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Klaus Barretto-Lopes

Investigators

  • Principal Investigator: Klaus B Lopes, PhD, Rio de Janeiro State University
  • Study Director: Kevin D O'Brien, PhD, University of Manchester
  • Study Chair: Jose Augusto M Miguel, PhD, Rio de Janeiro State University
  • Study Director: Nathália Palomares, MSc, Rio de Janeiro State University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2015

Primary Completion (Anticipated)

August 1, 2025

Study Completion (Anticipated)

September 1, 2025

Study Registration Dates

First Submitted

March 26, 2015

First Submitted That Met QC Criteria

April 7, 2015

First Posted (Estimate)

April 8, 2015

Study Record Updates

Last Update Posted (Actual)

October 27, 2022

Last Update Submitted That Met QC Criteria

October 24, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HASA

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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