Gum treatment may ease arthritis symptoms, study finds
NCT ID NCT02779179
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether treating gum disease (periodontitis) can reduce the severity of rheumatoid arthritis (RA) in people who have both conditions. Researchers enrolled 22 adults with RA and gum disease, providing periodontal treatment and measuring changes in RA activity over time. The goal was to see if addressing gum inflammation could help control arthritis symptoms.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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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22 people
The number who actually took part.
- Started
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Nov 2010
- Finished
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Nov 2016
- 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 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.
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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: * rheumatoid arthritis diagnosed for at least one year * DAS28 score between 3.2 and 5.1 * no change to medication, dosage or formulation in RA treatment during the 3 months preceding the screening visit * subject available for all study visits over three months in the Dental Care Departments (V1 to V4) * subjects with at least six natural teeth with root * subject with periodontitis, defined by the presence of one site with periodontal probing depth ≥ 4 mm and clinical attachment level ≥ 3 mm on at least 4 teeth. * subject has given his informed consent: 1 week cooling-off period EXCLUSION CRITERIA: * subject will not qualify for enrolment if he presents at least one of the following: acute oral infection, acute oral pain (including pulpitis), suspicious oral mucosal lesion, severe oral inflammation unrelated to periodontal conditions, or need for immediate tooth extractions * have a planned hospitalization within 4 months after the screening visit * subject suffering from one or more known infectious diseases (HIV, hepatitis, infectious mononucleosis), * subject suffering from known clinically significant renal disease (creatinine clearance \<60 ml/min), or liver disease, * unbalanced diabetes * have a known risk of endocarditis, * have a permanent pacemaker, * subject taking antithrombotic treatment, * subject having severe difficulties in understanding written and spoken French * for females: are pregnant or intending to become pregnant, or lactating * subject suffering from a chronic disorder that requires chronic or intermittent use of antibiotics, * subject having known hypersensitivity to chlorhexidine gluconate * are participating in another intervention study * have known contraindications to both amoxicillin and clindamycin * have known contraindications to dental local anesthetic.
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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
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CHU de Bordeaux
Bordeaux, 33000, France
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Pôle Odontologie Hôpital Purpan - Pavillon Rayer
Toulouse, 31059, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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