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Digital Quantification of Dental Plaque Based on Intraoral Scanner Images

Digital Quantification of Dental Plaque Based on Intraoral Scanner Images

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07152314
Enrollment
20
Registered
2025-09-03
Start date
2025-09-19
Completion date
2025-10-04
Last updated
2026-09-11

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

Conditions

Dental Plaque, Dental Plaque (Diagnosis), Dental Plaque Imaging Methods, Gingivitis, Periodontal Disease

Keywords

Dental Biofilm, Intraoral Scanner, Preventive Dentistry, Plaque quantification, Digital Diagnosis

Brief summary

This diagnostic validation study aims to develop and validate a digital method for dental biofilm quantification using three-dimensional images obtained by an intraoral scanner. Twenty participants will undergo intraoral scanning at three time points: before and after plaque disclosure, and after supervised toothbrushing. The digital method's accuracy will be compared with traditional clinical assessment methods (Turesky Plaque Index).

Detailed description

A prospective, evaluator-blinded clinical study including 20 participants (18-65 years) with at least 20 natural teeth and a visible plaque index \>20%. Participants will be evaluated at three time points in a single session using TRIOS 4 intraoral scanner. Digital analysis will be performed using Geomagic Control X software to calculate the percentage of surface area covered by plaque. The study includes standardized intraoral photographs and supervised toothbrushing procedures. This digital method aims to provide a more objective and precise assessment of dental biofilm, overcoming limitations of conventional visual assessment methods.

Interventions

DIAGNOSTIC_TESTDigital plaque quantification using intraoral scanner

Participants will undergo three-dimensional intraoral scanning at three time points during a single session: initial scanning (T0), after biofilm disclosure with plaque disclosing solution (T1), and after supervised toothbrushing (T2).

Sponsors

University of Guarulhos
Lead SponsorOTHER
Colgate Palmolive
CollaboratorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Presence of at least 20 natural teeth * Visible plaque index \> 20% at initial assessment * Age between 18 and 65 years * Both sexes eligible

Exclusion criteria

* Use of fixed orthodontic appliances * Presence of extensive restorations or fixed dentures on the anterior teeth * Systemic conditions that interfere with the formation of dental biofilm * Use of medications that alter salivary flow

Design outcomes

Primary

MeasureTime frameDescription
Correlation between digital 3D intraoral scans and traditional plaque assessment methodsSingle session (approximately 1.5-2 hours)Correlation between the percentage of dental surface area covered by biofilm quantified by the digital method (intraoral scanner) and the plaque index obtained by the traditional clinical method (Quigley-Hein Plaque Index modified by Turesky)

Secondary

MeasureTime frameDescription
Correlation between digital 2D images and traditional plaque assessment methodsSingle session (approximately 1.5-2 hours)Correlation between the percentage of dental surface area covered by biofilm quantified by intraoral photographs with different filters and the plaque index obtained by the traditional clinical method (Quigley-Hein Plaque Index modified by Turesky)
Fluorescence imaging capabilitiesSingle session (approximately 1.5-2 hours)Detection sensitivity for plaque, correlation with clinical findings, and reproducibility of fluorescence measurements.
Plaque volume changes analysisSingle session (approximately 1.5-2 hours)Ability of the digital method to detect changes in the amount of biofilm, evaluated by the percentage difference in area covered between T0 (initial), T1 (after disclosure) and T2 (after professional brushing).
Plaque thickness changes analysisSingle session (Approximately 1.5-2 hours)Ability of the digital method to detect changes in the amount of biofilm, evaluated by the color map difference in area covered between T0 (initial), T1 (after disclosure), and T2 (after professional brushing), and correlating those with other features, such as disclosing agent color and fluorescence.

Countries

Brazil

Contacts

PRINCIPAL_INVESTIGATORMohamed A Hassan, PhD

University of Guarulhos

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026