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Quantitative In Vivo Monitoring of Early Erosion-Associated Enamel Optical Changes Using Swept-Source Optical Coherence Tomography.

1 juli 2026 bijgewerkt door: Azwatee binti Abdul Aziz, University of Malaya

This study aims to evaluate the ability of swept-source optical coherence tomography (SS-OCT) to detect early enamel optical changes associated with erosive tooth wear under clinically relevant in vivo conditions. The study also investigates whether salivary stimulation induced by sugar-free chewing gum influences enamel optical properties following repeated erosive challenges.

A prospective, longitudinal, within-subject study with a fixed-sequence design was conducted. Twenty-two healthy adults aged 23-33 years participated after meeting predefined inclusion and exclusion criteria. All participants completed two sequential experimental phases separated by a two-day washout period. A fixed-order design (Phase A followed by Phase B) was selected to standardize erosive exposure and minimize variability during repeated intraoral OCT measurements. As an exploratory study, randomization was not performed.

In both phases, participants underwent repeated erosive challenges using commercially available orange juice (pH 3.4). During each challenge, participants swished 25 mL of orange juice for 30 seconds followed by a 30-second rest interval, repeated continuously for 10 minutes (total exposure: 250 mL). Erosive challenges were performed three times daily at three-hour intervals over three consecutive days under investigator supervision.

Phase A consisted of repeated erosive challenges without intervention. In Phase B, participants followed the identical erosive protocol but chewed sugar-free chewing gum for 15 minutes immediately after each erosive challenge to stimulate salivary flow and enhance natural buffering and remineralization mechanisms.

All participants used standardized fluoridated toothpaste and soft-bristled toothbrushes beginning two days before the study and throughout the experimental period. Unstimulated salivary flow rate was measured before enrolment, and participants with salivary flow rates below 0.2 mL/min were excluded.

The primary outcome measure was enamel integrated reflectivity (IR), quantified from SS-OCT A-scan analysis as an indicator of enamel optical changes associated with early demineralization. A commercially available swept-source OCT system equipped with an intraoral probe was used for image acquisition. The middle third of the labial surface of the maxillary right central incisor (tooth 11) served as the standardized imaging site. Custom acrylic positioning devices and anatomical landmarks were used to improve reproducibility of repeated measurements.

SS-OCT imaging was performed at six standardized time points during each study day: baseline before the first erosive challenge (t1), after the first challenge (t2), after the second challenge (t3), after the third challenge (t4), following a three-hour rest period (t5), and the following morning after overnight salivary exposure (t6). Image acquisition parameters, drying procedures, and positioning were standardized for all participants.

Integrated reflectivity values were calculated from predefined regions of interest using established OCT image analysis methods. Five adjacent A-scans were averaged to reduce signal noise. Statistical analyses included paired sample t-tests for predefined comparisons and linear mixed-effects modelling to evaluate longitudinal changes while accounting for repeated measurements within participants. Statistical significance was set at α = 0.05.

The study was approved by the appropriate institutional ethics committee, and written informed consent was obtained from all participants before enrolment. The study complied with the principles of the Declaration of Helsinki. Findings are expected to provide evidence regarding the feasibility of SS-OCT as a non-invasive clinical tool for monitoring early erosive enamel changes and evaluating preventive interventions under clinically relevant oral conditions.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

22

Fase

  • Niet toepasbaar

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

Healthy adults aged 23-33 years. Presence of intact maxillary right central incisor (tooth 11) suitable for repeated SS-OCT imaging.

Good general and oral health. Normal unstimulated salivary flow rate (≥0.2 mL/min). Willingness to comply with all study procedures, including repeated erosive challenges and SS-OCT examinations.

Provision of written informed consent prior to participation.-

Exclusion Criteria:

Presence of active dental caries, restorations, enamel defects, cracks, or erosive lesions on the study tooth.

Ongoing orthodontic treatment affecting the study tooth. History of systemic diseases or medications known to affect salivary flow or enamel mineralization.

Unstimulated salivary flow rate <0.2 mL/min. Pregnancy or breastfeeding. Known allergy or intolerance to orange juice or sugar-free chewing gum. Current smokers or tobacco users. Inability or unwillingness to comply with study procedures or attend all scheduled visits.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Diagnostisch
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Repeated Erosive Challenge With and Without Chewing Gum Stimulation
Participants underwent two sequential experimental phases in a fixed-order design. During Phase A, participants received repeated orange juice erosive challenges without chewing gum stimulation for three consecutive days. Following a two-day washout period, all participants completed Phase B, during which the identical erosive challenge protocol was repeated with 15 minutes of sugar-free chewing gum immediately after each erosive challenge. Swept-source optical coherence tomography (SS-OCT) imaging was performed repeatedly throughout both phases to monitor enamel optical changes. Each participant served as his or her own control.
A commercially available swept-source optical coherence tomography (SS-OCT) system (OCS1300SS, Thorlabs Inc., USA) equipped with an intraoral probe was used to obtain non-invasive cross-sectional images of enamel. The labial surface of the maxillary right central incisor was imaged under standardized conditions at six time points per day during each 3-day experimental phase to quantify enamel integrated reflectivity.
Participants swished 25 mL of commercially available orange juice (pH 3.4) for 30 seconds followed by a 30-second rest interval. This cycle was repeated continuously for 10 minutes (total exposure: 250 mL per session). The erosive challenge was performed three times daily at 3-hour intervals for three consecutive days during both experimental phases.
During Phase B, participants chewed one piece of sugar-free chewing gum (Wrigley's Extra® Peppermint) for 15 minutes immediately after each orange juice erosive challenge to stimulate salivary flow. This intervention was repeated after each of the three daily erosive challenge sessions over three consecutive days.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in enamel integrated reflectivity measured by swept-source optical coherence tomography (SS-OCT)
Tijdsspanne: Baseline through Day 3 of each study phase (6 measurements per day over two 3-day experimental phases).

Description

Integrated reflectivity (IR), derived from SS-OCT A-scan analysis, will be used to quantify changes in enamel backscattered light intensity associated with early erosion-related optical alterations. Higher IR values indicate increased optical scattering consistent with enamel demineralization.

Baseline through Day 3 of each study phase (6 measurements per day over two 3-day experimental phases).

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Longitudinal changes in enamel integrated reflectivity during repeated erosive challenges
Tijdsspanne: Baseline through Day 3 of each experimental phase.
Longitudinal changes in integrated reflectivity will be evaluated using repeated SS-OCT measurements and linear mixed-effects modelling to assess cumulative enamel optical changes over time and between experimental phases.
Baseline through Day 3 of each experimental phase.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

21 juni 2016

Primaire voltooiing (Werkelijk)

24 juni 2016

Studie voltooiing (Werkelijk)

30 juni 2016

Studieregistratiedata

Eerst ingediend

1 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

1 juli 2026

Eerst geplaatst (Werkelijk)

8 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

8 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

1 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • Ethics: DF RD1617/0054(P)
  • UM-MOHE HIR Grant UM.C/HIR/MOH (Ander subsidie-/financieringsnummer: Ministry of Higher Education, Malaysia)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Do not intend to make de-identified individual participant data publicly available.

The ethics approval and participant consent did not include provisions for sharing individual participant data.

Data will only be available upon reasonable request or not at all.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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