ClinicalTrials.gg
Active, not recruitingNCT07295977Updated Dec 22, 2025

Effect of Dehydration on Dental Fluorescence

An observational study in Evaluate the Fluorescence of Natural Tooth Following Dehydration, sponsored by Marmara University. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-22.

Sponsored by Marmara University · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
10
Ages
18 Years to 35 Years
Sex
All
01

Study summary

A cheek retractor will be placed to ensure consistent isolation throughout the procedure. Dehydration will be assessed at baseline, at the 5th minute, and at the 10th minute using three different evaluation techniques. At each time point, digital photographs will be captured under two distinct fluorescence light sources to document changes visually. In addition, fluorescence images will be obtained using the QLF (Quantitative Light-Induced Fluorescence) device to provide objective, quantitative data. All images will be recorded and analyzed digitally to evaluate dehydration-related changes in fluorescence. The aim of our study is to clinically evaluate the changes in the fluorescence properties of natural tooth following dehydration.

Read the detailed description

According to the power analysis, the required number of teeth was 69, with 95% statistical power and a 5% alpha error level. The study will be conducted at the Clinic of the Department of Restorative Dentistry, Marmara University Faculty of Dentistry. Individuals with caries-free teeth, no enamel defects, no restorations on tooth surfaces, no visible plaque, and adequate cognitive ability to read and understand the informed consent form will be included in the study. Those with teeth exhibiting discoloration or with systemic conditions or medication use that may cause structural changes on the tooth surfaces will be excluded. Maxillary and mandibular anterior teeth will be evaluated.

A cheek retractor will be placed in the patients' mouths, and baseline, 5th-minute, and 10th-minute dehydration will be evaluated using three different techniques. Digital photographs will be taken at baseline and post-procedure under two different fluorescence light sources (Ashur plaque indicator (405 nm), and Led lights (365 nm)), and the images obtained using the QLF (Quantitative Light-Induced Fluorescence- 405 nm) device will be recorded. Analyses will be carried out digitally. Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the LED lights (1/125, f/22, ISO 8000) and for the Ashur device (1/125, f/22, ISO 25600). To ensure standardization, the LED lights will be stabilized on the flash brackets at a 45° angle on both sides, and all images will be captured in a dark room. QLF images will be obtained with its own camera. The photographs and the QLF images will be analyzed using Adobe Photoshop software, and color changes will be determined based on ∆E values. For each method ∆E values will be calculated individually, there will be 3 different ∆E values (baseline and 5th-minute, baseline and 10th-minute, 5th-minute and 10th-minute). For ∆E calculations, the CIEDE2000 formula will be used, employing the measured L*, a*, b* and L*, c*, h* values obtained from baseline, 5th-minute and 10th-minute images. For the digital measurements, the intraobserver variability will be assessed, and after obtaining a high level of agreement, the study will be initiated. In statistical analyses, normality will be assessed using the Shapiro-Wilk test; repeated-measures ANOVA will be used if normal distribution is present, and the Friedman test will be applied if normality is not observed. A significance level of p\<0.05 will be accepted.

The aim of this clinical study is to clinically evaluate the changes in the fluorescence properties of natural teeth following dehydration.

The hypotheses of the study (H1) are as follows:

  1. The change in the fluorescence properties of natural teeth after dehydration exceeds clinically acceptable thresholds.
  2. There is a significant difference among the various fluorescence evaluation methods used in clinical practice.
02

Conditions studied

  • Evaluate the Fluorescence of Natural Tooth Following Dehydration

Browse trials for

Keywords

  • fluorescence
  • dehydration
  • teeth
03

In context

Dehydration

201 studies on the registry are indexed under Dehydration; 28 are open to participants now.

This study's planned enrollment of 10 is below the median of 105 across 46 observational studies indexed under Dehydration.

Browse Dehydration studies →

Lead sponsor

Marmara University is the lead sponsor of 599 studies on the registry; 138 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals with caries-free teeth, no enamel defects, no restorations on tooth surfaces, no visible plaque, and adequate cognitive ability to read and understand the informed consent form will be included in the study. Those with teeth exhibiting discoloration or with systemic conditions or medication use that may cause structural changes on the tooth surfaces will be excluded. Maxillary and mandibular anterior teeth will be evaluated.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals with caries-free teeth, no enamel defects, no restorations on tooth surfaces, no visible plaque, and adequate cognitive ability to read and understand the form.

Exclusion criteria

Exclusion Criteria:

  • Individuals with teeth exhibiting discoloration or with systemic conditions or medication use that may cause structural changes on the tooth surfaces.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
10 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • group 1

    Dehydration of teeth will be assessed at baseline, at the 5th minute, and at the 10th minute using three different evaluation techniques.

    Diagnostic Test: Digital photograph with Ashur plaque indicator · Diagnostic Test: Digital photographs with the Led lights (365 nm) · Diagnostic Test: The QLF (Quantitative Light-Induced Fluorescence- 405 nm) images

Interventions

  • Diagnostic testDigital photograph with Ashur plaque indicator

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Ashur plaque indicator (405 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the Ashur device (1/125, f/22, ISO 25600). To ensure standardization all images will be captured in a dark room.

  • Diagnostic testDigital photographs with the Led lights (365 nm)

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Led lights (365 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the LED lights (1/125, f/22, ISO 8000). To ensure standardization, the LED lights will be stabilized on the flash brackets at a 45° angle on both sides, and all images will be captured in a dark room.

  • Diagnostic testThe QLF (Quantitative Light-Induced Fluorescence- 405 nm) images

    The images obtained using the QLF (Quantitative Light-Induced Fluorescence- 405 nm) device will be recorded. QLF images will be obtained with its own camera.

06

What researchers measure

Primary outcomes

  1. Digital photograph with Ashur plaque indicator

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Ashur plaque indicator (405 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the Ashur device (1/125, f/22, ISO 25600). To ensure standardization all images will be captured in a dark room.

    Time frame: baseline

  2. Digital photographs with the Led lights (365 nm)

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Led lights (365 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the LED lights (1/125, f/22, ISO 8000). To ensure standardization, the LED lights will be stabilized on the flash brackets at a 45° angle on both sides, and all images will be captured in a dark room.

    Time frame: baseline

  3. The QLF (Quantitative Light-Induced Fluorescence- 405 nm) images

    The images obtained using the QLF (Quantitative Light-Induced Fluorescence- 405 nm) device will be recorded. QLF images will be obtained with its own camera. All images will be captured in a dark room.

    Time frame: baseline

  4. Digital photograph with Ashur plaque indicator

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Ashur plaque indicator (405 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the Ashur device (1/125, f/22, ISO 25600). To ensure standardization all images will be captured in a dark room.

    Time frame: at 5th minute

  5. Digital photographs with the Led lights (365 nm)

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Led lights (365 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the LED lights (1/125, f/22, ISO 8000). To ensure standardization, the LED lights will be stabilized on the flash brackets at a 45° angle on both sides, and all images will be captured in a dark room.

    Time frame: at 5th minute

  6. The QLF (Quantitative Light-Induced Fluorescence- 405 nm) images

    The images obtained using the QLF (Quantitative Light-Induced Fluorescence- 405 nm) device will be recorded. QLF images will be obtained with its own camera. All images will be captured in a dark room.

    Time frame: at 5th minute

  7. Digital photograph with Ashur plaque indicator

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Ashur plaque indicator (405 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the Ashur device (1/125, f/22, ISO 25600). To ensure standardization all images will be captured in a dark room.

    Time frame: at 10th minute

  8. Digital photographs with the Led lights (365 nm)

    Digital photographs will be taken at baseline and post-procedure under the fluorescence light source (Led lights (365 nm). Images will be captured with a Sony Alpha 7iii (Sony, Japan) digital camera equipped with a 90-mm macro lens. Camera settings will be adjusted for the LED lights (1/125, f/22, ISO 8000). To ensure standardization, the LED lights will be stabilized on the flash brackets at a 45° angle on both sides, and all images will be captured in a dark room.

    Time frame: at 10th minute

  9. The QLF (Quantitative Light-Induced Fluorescence- 405 nm) images

    The images obtained using the QLF (Quantitative Light-Induced Fluorescence- 405 nm) device will be recorded. QLF images will be obtained with its own camera. All images will be captured in a dark room.

    Time frame: at 10th minute

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — Data may be shared after the publication of the study

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2025 to primary completion in Jun 2025, 1 month.

Of 19 observational studies under Dehydration, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 30. This study's 1 month is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 8, 2025
First posted
Dec 22, 2025
StartActual
Apr 7, 2025
Primary completionActual
Jun 2, 2025
CompletionEst.
Dec 2025
Last update
Dec 22, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07295977
Lead sponsor
Marmara University
Responsible party
Sponsor
First posted
Dec 22, 2025
Start date
Apr 7, 2025
Primary completion
Jun 2, 2025
Completion
Dec 2025 (estimated)
Last update
Dec 22, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion