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Can a new device catch tooth decay before it becomes a cavity?
NCT ID NCT07819370
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Researchers are testing a device called BlueCheck to see if it can reliably find early enamel lesions and track how they change over 12 weeks. Participants aged 13 and older with active enamel lesions but no cavities needing immediate fillings receive high-fluoride toothpaste and have their teeth checked with BlueCheck, X-rays, and an intraoral camera. The goal is to learn whether BlueCheck gives consistent readings that could help dentists monitor early decay.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BlueCheck, a device that detects early tooth decay, plus high-fluoride toothpaste
- What this could lead to
- If BlueCheck works, dentists could catch early enamel damage sooner and track whether fluoride toothpaste is repairing it, possibly heading off cavities before they need drilling.
- What could go wrong
- This is a tiny study with only five participants, so results may not hold up in larger groups. BlueCheck might miss lesions or give inconsistent readings, and it is not yet clear whether spotting lesions earlier actually changes outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 5 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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13 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Signed Informed Consent/Assent Form. * Male and female subjects aged 13 years or older. * Availability for the duration of the study. * Good general health and good oral health based on the opinion of the study investigator. * Subjects must have active enamel lesions and no cavities requiring immediate restoration in the mouth. * Subjects must be candidates for high fluoride toothpaste treatment. Exclusion Criteria: * Subjects with fixed or removable orthodontic appliances or removable partial dentures. * Obvious signs of periodontal disease or any condition that the dental examiner considers exclusionary from the study. * Cavities. * Concurrent participation in another oral clinical study. * Self-reported pregnant and/or lactating women, or those planning to become pregnant during the study. * History of allergies or sensitivity to personal care consumer products or their ingredients. * Medical condition which requires premedication prior to dental visits/procedure. * Significant oral soft tissue pathology, excluding plaque-induced gingivitis. * Dental prophylaxis within 30 days prior to study start. * Subjects who must receive dental treatment during the study dates. * Immunocompromised individuals (HIV, AIDS, immunosuppressive drug therapy). * Use of smokeless tobacco, vaping, or e-cigarettes or suspected substance abuse. * Current smokers (if former smoker, should have stopped at least 1 month prior to Visit 1). * Subjects who have an infectious disease and/or other blood borne diseases (Hepatitis series, HIV, tuberculosis).
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Dental Dreams, LLC
Lithonia, Georgia, 30038, United States
Contact Email: •••••@•••••
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