Gum showdown: calibrated brushes may beat regular ones for healthy smiles
NCT ID NCT06848790
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using a calibrated interdental brush (sized to fit each gap) reduces gum bleeding better than a non-calibrated brush in 51 healthy young adults aged 18-30. Participants used one type of brush daily for three months. The main goal was to compare gum inflammation between the two groups. Results could help improve daily oral hygiene advice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- interdental brush (calibrated or non-calibrated)
- What this could lead to
- If calibrated brushes prove more effective, this could lead to clearer recommendations for preventing gum disease and related health issues.
- What could go wrong
- This is a small, completed trial with only 51 participants, so results may not apply to everyone. The study does not test long-term health 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
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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51 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Apr 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Person between 18 and 30 years old * Person who has given free, informed, express written consent * Person affiliated to a French social security system * Person living or working in Lyon or the Lyon conurbation served by public transport (TCL) Exclusion Criteria: * Person with a smoking addiction * Person participating in another study related to oral hygiene * Patients at high risk of infective endocarditis * Person with chronic pathologies * Person having taken antibiotic treatment during the month preceding the start of the study * Pregnant, parturient or breastfeeding woman * Persons deprived of liberty by a judicial or administrative decision * People receiving psychiatric care * Persons admitted to a health or social establishment for purposes other than research * Adults subject to a legal protection measure (guardianship, curatorship) * Persons not affiliated to a social security scheme or beneficiaries of a similar scheme * Person with fewer than 20 natural teeth * Person performing interdental hygiene and/or daily mouthwashes. * Person wearing orthodontic appliance * Person with periodontal disease (stage ≥ II periodontal lesions according to the Chicago 2017 classification (i.e. PD ≥ 4 mm, and/or CAL ≥ 4 mm) and/or generalized (\>30% of sites )), active caries or during dental care
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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.
Contacts and locations
Locations
-
Service de Soins Dentaires Et D'Odontologie
Lyon, France
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Other studies related to the condition(s) this trial covers.
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