New tooth-cleaning gadget aims to banish dental drill pain
NCT ID NCT07482280
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a special ultrasonic handpiece that sprays hydroxyapatite (a natural enamel mineral) can reduce tooth sensitivity during dental cleanings for people with gum disease. Forty adults with moderate to severe periodontitis had half their mouth cleaned with the new device and the other half with a standard ultrasonic tool. Researchers measured changes in gum pocket depth and sensitivity over 6 months to see if the new method is more comfortable and effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hydroxyapatite
- What this could lead to
- If effective, this could offer a gentler, less painful option for dental cleanings in people with gum disease.
- What could go wrong
- This is a small, completed trial with only 40 participants, so results may not apply to everyone. The improvement in sensitivity may be modest or not last long-term.
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
-
40 people
The number who actually took part.
- Started
-
Feb 2023
- Finished
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Feb 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
-
18 to 75 years
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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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 Form. * Male and female subjects, aged 18-75 years, inclusive. * Good general health (free of systemic diseases such as diabetes, HIV infection or genetic disorder, ongoing malignant disease of any type that could influence the outcome of the treatment and might interfere with the evaluation of the study objectives). * History of periodontitis staging III or IV grading B or C * At least 4 sites (split mouth 2 - 2) with probing depth ≥6 mm or pockets of 5 mm with bleeding on probing. * Previous periodontal non-surgical treatment at least 3 months maximum 6 months. * Availability for the 6-month duration of the study for an assigned subject. Exclusion Criteria: * Not willing to follow the agreed protocol. * Presence of orthodontic appliances. * Smokers more than 10 cigarettes per day * Tumors or significant pathology of the soft or hard tissues of the oral cavity. * Current radiotherapy or chemotherapy. * Pregnant women. * Current or past (within 3 months prior to enrollment) assumption of medications that may influence periodontal conditions and/or interfere with healing following
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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
-
Magda Mensi
Brescia, Lombardy, 25123, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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