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The Effect of Timing on Orthodontic Treatment

Primary Purpose

Malocclusion, Angle Class II

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Early headgear treatment
Sponsored by
University of Oulu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malocclusion, Angle Class II focused on measuring Early orthodontic treatment, Class II treatment, Orthodontic treatment outcome

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Angle Class II malocclusion
  • Overbite 5 mm or more

Exclusion Criteria:

  • Opening bite
  • Syndrome
  • Lateral malocclusion

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Early headgear treatment

    Later headgear treatment

    Arm Description

    Headgear treatment is initiated at the age of 7-8 years and continued as long as Class I occlusion is achieved

    Headgear treatment is initiated in the beginning of the growth spurt.

    Outcomes

    Primary Outcome Measures

    Normal occlusion, short treatment time
    Normal occlusion is measure as occusal contacts and overbite/overjet, but also on x-rays.

    Secondary Outcome Measures

    Patient compliance
    There may be differences in patient compliance when the treatment is done at different ages. Also the comparison of behavioral issues is important here.

    Full Information

    First Posted
    December 9, 2013
    Last Updated
    June 11, 2018
    Sponsor
    University of Oulu
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02010346
    Brief Title
    The Effect of Timing on Orthodontic Treatment
    Official Title
    The Effect of Timing on Orthodontic Treatment - Studied by Randomized Clinical Settings
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2005 (undefined)
    Primary Completion Date
    December 2019 (Anticipated)
    Study Completion Date
    December 2019 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The aim of this longitudinal randomized investigation is to determine the long-term effects of early headgear treatment on craniofacial structures and dental arches, compared to treatment started later, during the most active growth period in Class II patients. The aim was further to find out the possible benefits and the burden of early treatment to the patients and parents of these common malocclusions, when compared to groups treated later, but with the same methods as much as possible. The hypothesis is that the timing of treatment has significant effects on orthodontic treatment total time, the general outcome of the treatment, and the compliance of the patient.
    Detailed Description
    Background In spite of the fact that about 30 to 50% of the children in Europe undergo orthodontic treatment during growth, negligible amount of evidence based data is available concerning these treatments. The most used treatment method in Finland, and one of the most popular in the world, is to treat dental crowding and class II malocclusion with the headgear (Mäntysaari et al., 2004; Pirttiniemi et al., 2005; Pietilä et al., 2008). The goal of the HG treatment is variously listed as to inhibit maxillary growth, to stimulate mandibular growth, or to ease the crowding. During the recent years McNamara (2002) and Fenderson et al (2004) have emphasized the advantages of the lateral expansion of dental arches in the treatment of crowding, especially stressing the stability of the results. The views of the effects of cervical headgear (HG) are to some extent obscure, at least when the long-term effects are concerned. Most reports that are based on a short-term follow-up, describe a restricted maxillary anterior growth. During the later growth, it is not clear what is the general association of early orthodontic treatment on crowding, but our earlier results show that in the final outcome there is no significant difference in stability of the treatment if crowding is treated with early headgear or later with fixed appliances only, at least when the long-term effects of the treatment are concerned (Krusinkiene et al., 2008). A valid evidence based data is rare and the thus exact conclusions are very difficult to be set (Petrén and Bondemark, 2008). Preliminary Studies We conducted a randomized clinical study with an early headgear treatment, where the control group was treated with a camouflage treatment in the adolescence. The main difference between the groups was broader dental arch with less extractions in the headgear group, the differences between the groups being relatively small when the craniofacial differences or the stability are concerned (Mäntysaari et al.,2004; Pirttiniemi et al.,2005; Krusinskiene et al., 2008). There were, however, some distinct profile differences between the groups and the canine eruption pattern was found to be more favorable in the early headgear group (Silvola et al., 2008; Virkkula et al., 2008). Experimental Design and Methods The Age cohort of six-year-old of children living in the community areas of Kemi, and Oulunsalo are screened at the age of 6 years for malocclusions. Of these children 120 children who meet the criteria are chosen for the study after the written consent. The inclusion criteria are Class II malocclusion, Overbite 5 mm or more. Exclusion criteria are openbite tendency as verified in cephalometry, missing permanent teeth, lateral malocclusion, or craniofacial anomaly. The children are randomized into two groups. In the first group the treatment with headgear device (GAC, Islandia, NY, USA) is started at the age of 7 to 8 years, and continued until Class I occlusion is achieved. In the second group headgear treatment is started before the pubertal growth spurt, verified by standing height measurements. In both groups all the necessary orthodontic treatment is done with fixed appliances, after the headgear treatment, when found necessary. -In both groups dental casts, cephalograms, and standardized profile and facial photograps are taken before treatment (T0), after the first treatment phase (T1), after the second treatment phase (T2) and after the growth (T3). Facial 3D scanning is performed for all the subjects after the treatment to find out the effect of different treatment methods on facial characteristics. The dental casts are scanned to make 3D models of the cast to be used in detailed analysis. A wide multi-level questionnaire is performed before, during and after the study to the parents and the children to find out the comprehensive effects of orthodontic treatment on the well-being of the child. The questionnaire includes the Rutter's child behavioural pattern (Rutter et al., 2001). In both studies, all the guidelines of RCT are applied (Moher and Schulz, 2005). Blinding of the clinicians is gained, as the orthodontists or dentists treating the children are not aware of the rationale of the study. Blinding is applied on all measurement of the documents. Quality assurance plan Quality of the data collected is secured by preliminary training that has been done concerning the input data and the registration processes. The collected data is monitored on regular basis, on clinical records this is done by three months intervals. The quality assurance of the clinical data is done by the same person who has trained the dental personnel by on-site monitoring and auditing. Immediate feed-back is given to the registering personnel concerning the quality of the records. The input data is monitored by testing the normality of the data during the input process. Immediate feed-back is given to the personnel doing the registration process in the cases of deviation is found in the range of normality or consistence of the data. Basic assumption is that the input data is supposed to be normally distributed with this type of patient material. Intra- and Inter-examiner error is tested during the measuring process to test the accuracy of the measurements. The level of error is compared to the level of level reached in corresponding studies. Sample size assessment Power and sample size calculation was made using the data derived from the preliminary studies (Mäntysaari et al., 2004), and the applied sample size was gained using the formula for the purpose:(http://stat.ubc.ca/~rollin/stats/ssize/n2.html). The used estimates for means and deviations were gained from the analogous preliminary study. The test power used in the power analysis was 0.80 with the level of significance p=0.05. The used value give the sample size 49, and thus the used sample is very sufficient. Plan for missing data It is known from earlier longitudinal orthodontic studies that the drop-out rate is about 20% when reaching the end point of the study. This has been taken into account in the original sample size. As randomization is applied, it is likely that the missing subjects will occur approximately at the same rate in both study groups and by choosing appropriate statistical methods, the data can be handled. Statistical analysis plan The study hypothesis is tested by using statistical methods. When the differences between the two groups are tested, a test for two independent samples is utilized. When the values of the children are compared at different time points, a test of related samples is used. If the sample data is not normally distributed, a non-parametric test is applied ( e.g. Mann-Whitney-test or Wilcoxon-test). When the behavioral items are tested, the applied tests are on ordinary level or nominal level (e.g. Cross-tabulation tests). To estimate the Intra-examiner and Inter-examiner error, double measurements are performed. The statistical testing of the error is done using Intra class correlation (ICC). The Intention to treat principle is applied in the study The results will be shown both in graphical and table format to clearly show group and individual variation. The statistical testing is done by using the latest version of SPSS program. Timing and Importance of the studies The first part of the study (the headgear study) has begun in 2005. The study will continue actively during the years 2005-2014. The treatments and the follow-up continues until the growth is over, until about year 2018, and further until the adulthood. Most of the data, however, is available to be analyzed already earlier in 2013-2014. The results of these studies are clinically very important and therefore they will be published in the most respected international orthodontic journals. As the results are of the highest clinical relevance with a sound evidence, they can easily be applied directly to clinical practices. University of Oulu will give all the facilities needed for the research, including rooms. The clinical examinations are performed in the health centers as a part of normal treatment costs, when normal documentation is concerned. REFERENCES E. Literature Cited: Fenderson FA, McNamara JA Jr, Baccetti T, Veith CJ. A long-term study on the expansion effects of the cervical-pull facebow with and without rapid maxillary expansion. Angle Orthod 2004;74:439-449. Krušinskienė V, Kiuttu P, Julku J, Silvola A-S, Kantomaa T, Pirttiniemi P. A randomized controlled study of early headgear treatment on occlusal stability - a 13 year follow- up. Eur J Orthod 2008;30:418-24 McNamara JA Jr. Early intervention in the transverse dimension: is it worth the effort? Am J Orthod Dentofacial Orthop 2002;121:572-4. Moher D, Schulz KF, Altman D. The CONSORT Statement: revised recommendations for improving the quality of reports of parallel-group randomized trials 2001.Explore 2005;1:40-5. Mäntysaari R, Kantomaa T, Pirttiniemi P, Pykalainen A. The effects of early headgear treatment on dental arches and craniofacial morphology: a report of a 2 year randomized study. Eur J Orthod 2004;26:59-64. Petrén S, Bondemark L.Correction of unilateral posterior crossbite in the mixed dentition: a randomized controlled trial.Am J Orthod Dentofacial Orthop. 2008;133:790.e7-13. Pietilä I, Pietilä T, Pirttiniemi P, Varrela J, Alanen P. Orthodontists' views on indications for and timing of orthodontic treatment in Finnish public oral health care. Eur J Orthod 2008;30:46-51 Pirttiniemi P, Kantomaa T, Mantysaari R, Pykalalinen A, Krusinskiene V, Laitala T, Karikko J. The effects of early headgear treatment on dental arches and craniofacial morphology: an 8 year report of a randomized study. Eur J Orthod 2005;27:429-36 Rutter M, Pickles A, Murray R, Eaves L.Testing hypotheses on specific environmental causal effects on behavior. Psychol Bull 2001;127:291-324. Sivola AS, Arvonen P, Julku J, Lähesmäki R, Kantomaa T, Pirttiniemi P. Early headgear effects on the eruption pattern of the maxillary canines. Angle Orthodont 2009;79:540-5 Virkkula T, Kantomaa T,Julku J, Pirttiniemi P. The long-term soft-tissue response to orthodontic treatment with early cervical headgear - a randomized study. Am J Orthod Dentofac Orthoped 2009;135:586-96

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Malocclusion, Angle Class II
    Keywords
    Early orthodontic treatment, Class II treatment, Orthodontic treatment outcome

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Early headgear treatment
    Arm Type
    Experimental
    Arm Description
    Headgear treatment is initiated at the age of 7-8 years and continued as long as Class I occlusion is achieved
    Arm Title
    Later headgear treatment
    Arm Type
    No Intervention
    Arm Description
    Headgear treatment is initiated in the beginning of the growth spurt.
    Intervention Type
    Procedure
    Intervention Name(s)
    Early headgear treatment
    Other Intervention Name(s)
    Early orthodontic treatment, Orthodontic face bow, US patent: US 4212637 A, GAC 08-433-00 (NY,USA)
    Intervention Description
    The treatment with headgear is done as early treatment, beginning at ages 7-8 (Arm 1), or later, durning the maximal growth (arm 2)
    Primary Outcome Measure Information:
    Title
    Normal occlusion, short treatment time
    Description
    Normal occlusion is measure as occusal contacts and overbite/overjet, but also on x-rays.
    Time Frame
    10 years
    Secondary Outcome Measure Information:
    Title
    Patient compliance
    Description
    There may be differences in patient compliance when the treatment is done at different ages. Also the comparison of behavioral issues is important here.
    Time Frame
    10 years
    Other Pre-specified Outcome Measures:
    Title
    Stability of occlusion in adulthood
    Description
    The long-term outcome of the results, and also the satisfaction of the patients is important and can be measured at adulthood.
    Time Frame
    15 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Angle Class II malocclusion Overbite 5 mm or more Exclusion Criteria: Opening bite Syndrome Lateral malocclusion
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Pertti M. Pirttiniemi, Professor
    Organizational Affiliation
    University of Oulu, Finland
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    31369675
    Citation
    Julku J, Pirila-Parkkinen K, Tolvanen M, Pirttiniemi P. Comparison of effects of cervical headgear treatment on skeletal facial changes when the treatment time is altered: a randomized controlled trial. Eur J Orthod. 2019 Nov 15;41(6):631-640. doi: 10.1093/ejo/cjz053.
    Results Reference
    derived
    PubMed Identifier
    30601990
    Citation
    Julku J, Hannula M, Pirila-Parkkinen K, Tolvanen M, Pirttiniemi P. Dental arch effects after early and later timed cervical headgear treatment-a randomized controlled trial. Eur J Orthod. 2019 Nov 15;41(6):622-630. doi: 10.1093/ejo/cjy083.
    Results Reference
    derived
    PubMed Identifier
    29228206
    Citation
    Julku J, Pirila-Parkkinen K, Pirttiniemi P. Airway and hard tissue dimensions in children treated with early and later timed cervical headgear-a randomized controlled trial. Eur J Orthod. 2018 May 25;40(3):285-295. doi: 10.1093/ejo/cjx088.
    Results Reference
    derived

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