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A Comparison of the Alignment Achieved Using Computer-guided Indirect Bonding of Orthodontic Brackets to Conventional Appliance Placement

A Prospective Clinical Trial Comparing the Alignment Achieved Using Computer-guided Indirect Bonding of Orthodontic Brackets to Conventional Orthodontic Appliance Placement

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02221856
Enrollment
30
Registered
2014-08-21
Start date
2017-02-08
Completion date
2018-05-31
Last updated
2017-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malocclusion

Keywords

Conventional orthodontic treatment, Motion View

Brief summary

Technological advances have made computer aided orthodontic treatment planning possible. 3D dental scanners and software make it possible to design and approve the outcome before treatment begins. Manufacturers have provided different customized appliance systems that would help practitioners achieve those computer-designed outcomes. The purpose of this study is to determine the accuracy of computer-guided indirect bonding of orthodontic brackets at achieving the predicted alignment and comparing that to the accuracy of conventional orthodontic bracket placement at achieving a predetermined goal. The results of this study will help orthodontists and patients know if there is an advantage to using custom appliances. The study will be a prospective clinical study and will include a total of 60 arches from 30 patients enrolled at the Harvard School of Dental Medicine. 15 patients will be assigned to each of the two study groups (Motion View or control). Both groups will have a 3D intra-oral scan to measure the initial discrepancy and determine the computer-simulated design that the orthodontist believes is the optimized outcome. At the end of each patient's participation, a 3D intraoral scan will be taken and used to assess intra-arch leveling and alignment using ABO's objective grading system's criteria for alignment, marginal ridges and buccolingual inclination. Each arch will then be superimposed on the predicted outcome to determine how accurate each system was at achieving the planned movements in all 3 dimensions. We hypothesize that the accuracy of computer-guided indirect bonding (Motion View) at achieving the predicted outcomes will differ in comparison to the accuracy of conventional orthodontic bracket placement at achieving a predetermined goal.

Interventions

PROCEDUREMotion View

Motion View, a software we are using to place brackets virtually on a 3D rendition of a patients teeth, will be used to indirectly bond brackets onto patient's teeth with a 3D printed plastic transfer JIG in which the brackets will be precisely placed on the patients teeth according to the computer-guided software.

orthodontic treatment using non-customized brackets and stock wires

Sponsors

Harvard School of Dental Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects seeking orthodontic care * All permanent teeth must be erupted, excluding second and third molars * Class I, II, and III cases * No more than 7 mm crowding * No more than 45 degrees of rotations

Exclusion criteria

* Presence of systemic disease * Craniofacial anomalies, including cleft lip and palate * Syndromes affecting bone or teeth * Congenitally missing teeth, excluding third molars * Presence of bridges or implants * Periodontal disease * Use of drugs affecting tooth movement or bone metabolism (NSAIDS, bisphosphonates, PTH, corticosteroids) * Pregnancy

Design outcomes

Primary

MeasureTime frame
Discrepancy between predicated and actual tooth positionsup to 12 months

Secondary

MeasureTime frame
assessed quality of treatment measured by the American Board of Orthodontics (ABO) objective grading systemup to 12 months

Countries

United States

Contacts

Primary ContactMohamed Masoud, BDS, DMSc
Mohamed_Masoud@hsdm.harvard.edu617-432-4281

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026