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Alveolar Bone LossNCT04971642

Intraoral Ultrasound Imaging of Tooth-periodontium Complex

A study testing Intraoral ultrasound in people with Alveolar Bone Loss and Periodontitis, 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

Misaligned teeth are very common in the population and are commonly known as malocclusion. This happens when the upper teeth do not align properly with the lower teeth. It can lead to difficulty in jaw movement, chewing, speech, and gum disease. Correction of malocclusion requires orthodontic (braces) treatment. Read more about this study

Who is it for?
Ages 10 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Alveolar Bone Loss, Periodontitis
What is being tested?
Intraoral ultrasound
Could I receive a placebo?
No, everyone receives an active treatment
How many people
64 participants
Where
1 siteCanada
Study dates
10 Feb 2021to 15 Jan 2023
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 10 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Participants will be recruited to the Orthodontic Clinic-Oral Health Clinic at the Department of Dentistry - University of Alberta based on the following inclusion criteria:
  • Males or females in the age group of 10-60 years old
  • Individuals with permanent dentition
  • Dental malocclusion with mild to moderate crowding
  • Individuals undergoing CBCT imaging as part of Orthodontic diagnostic records Individuals in the age group of 10-60 years would have a full complement of permanent teeth erupted which will help standardize the research methodology to prevent an error in data acquisition, caused by the overlap of dental tissue in the mixed dentition period.

Who cannot join

  • Participants with missing permanent teeth, gingival recession (below CEJ), severe crowding, or a history of corrective orthodontics will be excluded. Any co-factors (previous orthodontic treatment) that might influence the ultrasound findings, will be excluded. Participants with unfavorable oral hygiene will be excluded due to the ambiguity associated with data acquisition in an inflamed periodontium. Also, participants presenting with craniofacial syndromes will be excluded due to the factors related to changes in craniofacial anatomy (maxilla-mandible anatomy)

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Oral Health Clinic, 8th Floor, Kaye Edmonton Dental Clinic.

    Edmonton, Alberta, T6G 1Z1

Other trials in Canada

About this study

Official title: Ultrasound Imaging of Tooth-periodontium Complex Using an Innovative Intraoral Transducer

Misaligned teeth are very common in the population and are commonly known as malocclusion. This happens when the upper teeth do not align properly with the lower teeth. It can lead to difficulty in jaw movement, chewing, speech, and gum disease. Correction of malocclusion requires orthodontic (braces) treatment. Currently, the imaging technique known as cone-beam computed tomography (CBCT) has been routinely used in orthodontic diagnosis and treatment planning for patients with malocclusion. Although CBCT provides better information than conventional dental X-rays, it typically delivers more harmful radiation to the patients. This is especially important as radiation from repeated X-ray imaging during dental monitoring visits can be cumulative.

Ultrasound is commonly used in medical imaging. The ultrasound method is non-invasive, cost-effective, and free of ionizing radiation. The application of ultrasound has been investigated in many fields in Dentistry. We plan to evaluate the ability of intra-oral ultrasound to see the bone and gingiva around the tooth for patients under orthodontic treatment. If ultrasound is found to be a reliable tool in imaging the tooth-gum complex, children and adolescents will benefit immensely from the decreased radiation risks and reduced cancer rate.

Read the detailed description

Purpose:

The purpose of this study is to investigate a intraoral ultrasound to image the tooth-periodontium complex that is an alternative to ionizing radiation CBCT imaging.

Hypothesis:

Ultrasound imaging is a radiation-free alternative to image tooth-periodontium complex.

Justification:

Straight teeth and a healthy smile is paramount to an individual's well-being. Malocclusion (crowding of teeth) is the third most common dental anomaly according to the World Health Organization(WHO). The severity of malocclusion can cause difficulty in jaw movement, chewing, speech, and high susceptibility to gum disease. Correction of malocclusion problems requires comprehensive orthodontic treatment. CBCT imaging for orthodontic diagnosis and treatment planning has increased of late due to its inherent advantages over the traditional 2D planar cephalometric and panoramic radiography. These include the advantage of having 3D capabilities to view images with no superimposition or magnification errors. This is especially significant in detecting bony dehiscence and fenestration associated with orthodontic treatment. The presence of these defects decreases bony support to the teeth, which compounded with plaque-induced inflammation, can be detrimental to the health of the teeth during orthodontic tooth movement. CBCT image typically delivers much higher radiation than conventional dental radiographs. Orthodontic patients, mostly children, are increasingly susceptible to deleterious effects of ionizing radiation due to the accumulated radiation dose from repeated monitoring visits. Hence new imaging modalities such as ultrasound have been researched as a radiation-free alternative to CBCT imaging. The ultrasound technique uses echoes of mechanical waves and the acoustic properties of the target to produce an image non-invasively. The characteristics of the returning echoes are mainly governed by the elastic 'properties of the transmitting medium and the acoustic impedance contrast of the interface between the target and the surrounding medium. For decades, medical ultrasound has mainly been used to image soft tissues. Although the use of ultrasound in dentistry focused more on imaging dental hard tissues, most recently, its use has been expanded to image periodontal soft and hard structures. Although the interest in using ultrasound in dentistry is increasing, research on the use of ultrasound to study tooth-periodontal tissues is limited.

Objectives:

The objective of this study is to determine the validity and reliability of an intra-oral ultrasound technique in a clinical setting by comparing the ultrasound measurements with those of the clinical standard CBCT imaging.

Research Method/Procedures:

Participant recruitment:

60 orthodontic participants in the age group of 10-60 years old will be recruited for the study for over a year. This population group is screened and recruited from the patients seen at the Orthodontic Clinic in the Oral Health Clinic - Department of Dentistry based on the inclusion and exclusion criteria. Each subject will have diagnostic records taken as part of routine orthodontic diagnosis and treatment planning. These records include extraoral and intraoral photos, digital models, and CBCT imaging. In addition to routine diagnostic records, ultrasound scanning of the mandibular and maxillary incisor, canine, premolar, and molar teeth for a total of sixteen (16) teeth (four (4)teeth in each of the four quadrants) will be performed after obtaining informed consent from patients and their guardians. Following diagnostic records, all subjects will undergo orthodontic treatment for correction of their malocclusion by either a licensed orthodontic faculty member or an orthodontic resident under the supervision of a licensed orthodontist at Kaye Edmonton Dental Clinic, University of Alberta.

Procedures:

Ultrasound Scanning:

The ultrasound scanner used is a handheld medical diagnostic system that has a Clarius platform (ClariusMobile Health, Richmond, Canada, Device ID: 1012444 and DeviceIdentifier 99-02-00046

) and a DenSonics DSI-1 intraoral 20 MHz array transducer (DenSonics Imaging Inc, Edmonton, Canada) to be used off-label (Health Canada has not approved yet).

All ultrasound scans will be done by the same research assistant after training. This research assistant has no involvement in the patient's care. The ultrasound imaging will be performed on the maxillary and mandibular(again 16 teeth per patient will be imaged - incisor/canine/premolar/molar in each of the four dental quadrants). The tooth-periodontium complex will be imaged.

The probe will be isolated for infection control using a plastic wrap and will be positioned intraorally with a gel pad separating the ultrasound transducer and the targeted tooth-periodontium structures, with the long axis of the probe in alignment with the longitudinal axis of the tooth. On average, it takes about 1-2 minutes to perform a single scan, and we estimate a total of 25 minutes to perform scans on all the teeth in a single individual. The saved data will be exported to a desktop computer for data analysis and measurements using in-house developed MATLAB codes.

Plan for Data Analysis:

Outcome measures:

The following five distance, thickness, or localization parameters will be measured linearly on ultrasound images for further analysis and comparison: (1) gingival margin- cementoenamel junction, (2) cementoenamel junction - alveolar bone crest, (3) gingival thickness at the alveolar bone crest, (4) alveolar bone thickness at the crest and (5) localization of cementoenamel junction. Measurements of the above five parameters will be performed by four raters in the ultrasound images. All the raters will be blinded for data processing and measurement. To test intra-rater reliability, each rater will conduct the measurement three times with one week apart between measurements to avoid bias. Three of the measurements: (2) cementoenamel junction - alveolar bone crest, (4) alveolar bone thickness at the crest and (5) localization of cementoenamel junction will be identified in both CBCT and ultrasound images and compared.

Statistical analysis:

Descriptive statistics will be presented as Mean±SD. Quality control of the data will be done by scatter plots to detect outliers. We will consider three assessments: Intra-rater reliability, inter-rater reliability, and agreement between the two methods. The intra- and inter-rater reliabilities will be assessed by intra-class correlation coefficients (ICC(2,1)) using a 2-way random model and absolute agreement with a 95% confidence interval. Correlation and the Bland-Altman plot will be used to assess the agreement between CBCT and ultrasound.

Being tested
Intraoral ultrasound
Keywords
ultrasound, periodontium
Medical subject headings
Alveolar Bone Loss, Periodontitis

What participants receive

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

  • Intraoral ultrasoundDevice

    Intraoral ultrasound scanning of the periodontium complex

Study groups in NCT04971642
Study groupRoleWhat they receive
Ultrasound scanningExperimentalThe subjects recruited are existing patients of the Orthodontic Clinic - Oral Health Clinic-Dentistry, University of Alberta. An intraoral ultrasound scanning will be done on the buccal side of the upper and lower incisor/canine/premolar/molar teeth for a total of sixteen (16) teeth (four(4) teeth in each of the four quadrants) of these subjects. The ultrasound scans will be done separately by a research assistant not involved in patient care. The whole procedure for ultrasound scanning and data storage will take about 25-30 min including 3-5 min preparation time and 22-25 min of data acquisition and storage time.
Receives: Device: Intraoral ultrasound

What is being measured

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

  1. Distance from alveolar bone crest to the cemento-enamel junction

    It is the linear measurement distance in millimeters (mm) from the alveolar bone crest to the cemento-enamel junction anatomical structures observed in the Ultrasound image. It will be evaluated using an image software.

    Measured: through study completion, an average of 1 year

  2. Distance from cemento-enamel junction to the gingival margin

    It is the linear measurement distance in millimeters (mm) from the cemento-enamel junction to the gingival margin observed in the Ultrasound image. It will be evaluated through an image software.

    Measured: through study completion, an average of 1 year

  3. Gingival thickness

    It is the linear measurement of the thickness of gingival tissue at the alveolar bone crest level in millimeters (mm) observed in the Ultrasound image. It will be evaluated using an image software

    Measured: through study completion, an average of 1 year

  4. Alveolar bone thickness

    It is the linear measurement of the alveolar bone thickness at the alveolar bone crest level in millimeters (mm) observed in the Ultrasound image. It will be evaluated using an image software.

    Measured: through study completion, an average of 1 year

  5. Cemento-enamel junction identification

    The Identification of the cemento-enamel junction will be done by adding a point to this anatomical structure in the ultrasound image. It will be evaluated using an image software

    Measured: through study completion, an average of 1 year

Timeline

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

  1. First posted21 Jul 2021
  2. Study start10 Feb 2021
  3. Primary completion28 Jul 2021
  4. Study completion15 Jan 2023

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
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
64 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04971642
Sponsor's protocol ID
Pro00099721
Status last verified
Sep 2024
First submitted
30 Apr 2021
Last updated
19 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data won't be shared for confidentiality reasons

Publications

  • Nguyen KCT, Duong DQ, Almeida FT, Major PW, Kaipatur NR, Pham TT, Lou EHM, Noga M, Punithakumar K, Le LH. Alveolar Bone Segmentation in Intraoral Ultrasonographs with Machine Learning. J Dent Res. 2020 Aug;99(9):1054-1061. doi: 10.1177/0022034520920593. Epub 2020 May 11.

    PubMed 32392449
  • Nguyen KT, Le LH, Kaipatur NR, Zheng R, Lou EH, Major PW. High-Resolution Ultrasonic Imaging of Dento-Periodontal Tissues Using a Multi-Element Phased Array System. Ann Biomed Eng. 2016 Oct;44(10):2874-2886. doi: 10.1007/s10439-016-1634-2. Epub 2016 May 9.

    PubMed 27160674
  • Nguyen KC, Le LH, Kaipatur NR, Major PW. Imaging the Cemento-Enamel Junction Using a 20-MHz Ultrasonic Transducer. Ultrasound Med Biol. 2016 Jan;42(1):333-8. doi: 10.1016/j.ultrasmedbio.2015.09.012. Epub 2015 Nov 3.

    PubMed 26546266
  • Nguyen KT, Pacheco-Pereira C, Kaipatur NR, Cheung J, Major PW, Le LH. Comparison of ultrasound imaging and cone-beam computed tomography for examination of the alveolar bone level: A systematic review. PLoS One. 2018 Oct 3;13(10):e0200596. doi: 10.1371/journal.pone.0200596. eCollection 2018.

    PubMed 30281591

Questions about this trial

What is this clinical trial studying?

A study testing Intraoral ultrasound in people with Alveolar Bone Loss and Periodontitis, 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 5 inclusion and 1 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 19 Sep 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?

Distance from alveolar bone crest to the cemento-enamel junction (time frame: through study completion, an average of 1 year). The study lists 5 primary outcomes in all. 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 NCT04971642, which also lists 4 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 19 Sep 2024.

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Clinical Trial NCT04971642 | AzTrials