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The effect of the treatment of periodontitis on rheumatoid arthritis disease activity

The effect of the treatment of periodontitis on rheumatoid arthritis disease activity in patients who referred to Rheumatology clinic, Semnan

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015122512823N3
Enrollment
30
Registered
2016-01-04
Start date
2016-01-05
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Periodontitis. Condition 2: Rheumatoid arthritis. Chronic periodontitis Rheumatoid arthritis, unspecified

Interventions

Interventions: At first, DAS-28 questionnaire filled and if periodontitis confirmed by dentist, treatment initiated which is includes non surgical scaling, root planning, systemic antibiotics (metroni
Treatment - Other

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18 years and older; diagnosis of RA at least one year ago; disease activity score between 3.2 and 5.1; having at least six natural teeth; the patient be educable; having gingivitis with mild to moderate degree. The exclusion criteria were: risk of infection; serious liver or kidney diseases; chronic infectious disease that needs to frequent use of antibiotics; uncontrolled diabetes; taking anti-thrombotic and biologic therapy; sensitivity to chlorhexidine gluconate (oral rinse); contraindication of amoxicillin and metronidazole; severe oral problems which requiring immediate surgery; pregnancy, breast-feeding or if want to get pregnant during the study period; any febrile or chronic diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Rheumatoid arthritis activity. Timepoint: Before initiation of interventions, 45 and 90 days after intervention. Method of measurement: DAS-28 questionnaire.

Secondary

MeasureTime frame
Erythrocyte Sedimentation Rate. Timepoint: Before initiation of interventions, 45 and 90 days after intervention. Method of measurement: Laboratory test.;C- reactive protein. Timepoint: Before initiation of interventions, 45 and 90 days after intervention. Method of measurement: Laboratory test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Jamileh Moghimi

Semnan University of Medical Sciences

moghimi_jam@yahoo.com+98 23 3343 7821

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026