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Gum treatment may ease arthritis symptoms, study finds

NCT ID NCT02779179

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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

22 people

The number who actually took part.

Started

Nov 2010

Finished

Nov 2016

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 years and older

Sex

Anyone

Healthy volunteers

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

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

  • CHU de Bordeaux

    Bordeaux, 33000, France

  • Pôle Odontologie Hôpital Purpan - Pavillon Rayer

    Toulouse, 31059, France

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Other studies related to the condition(s) this trial covers.