Can a DNA-Enriched mouthwash tame gum disease biofilm?
NCT ID NCT06028867
First seen Aug 07, 2026 · Last updated Aug 12, 2026 · Updated 2 times
Summary
This trial tests whether a mouthwash containing chlorhexidine and sodium DNA can better control bacterial biofilm in people with advanced periodontitis (stage III or IV). Participants will receive standard non-surgical gum treatment plus one of two mouthwashes or a placebo, and researchers will compare their effects on subgingival biofilm after two weeks. The goal is to see if the sodium DNA formulation offers extra antimicrobial benefits over chlorhexidine alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Chlorhexidine 0.12% + Sodium DNA mouthwash
- What this could lead to
- If effective, this mouthwash could become a simple at-home addition to gum disease treatment, helping to control bacterial biofilm and improve outcomes.
- What could go wrong
- This is a small, early-stage trial, so results may not be conclusive or widely applicable. The mouthwash may not outperform standard care, and side effects like tooth staining are possible with chlorhexidine.
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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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66 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Apr 2024
- Lead sponsor
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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 to 75 years
- 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: • Clinically diagnosed with stage III or IV periodontitis according to the EFP/AAP 2017 criteria. Exclusion Criteria: * Periodontal treatment, antibiotics, NSAIDs, immunosuppressants during the last 6 months. * Pregnancy. * Systemic diseases.
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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
-
AOU Policlinico G. Rodolico
Catania, Italy, 95124, Italy
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Other studies related to the condition(s) this trial covers.
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