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Rheumatoid Arthritis and Treatment of Periodontitis: a Randomized Clinical Trial.

U

University of Pisa

Status

Completed

Conditions

Periodontitis
Arthritis, Rheumatoid

Treatments

Procedure: Immediate non-surgical periodontal treatment and oral hygiene instructions

Study type

Interventional

Funder types

Other

Identifiers

NCT05271890
Perioreuma

Details and patient eligibility

About

Periodontitis is an infectious disease defined by bacteria-mediated inflammation of the supporting tissues of the teeth that if left untreated may ultimately lead to the destruction of the attachment apparatus, culminating in tooth loss. Rheumatoid arthritis is a chronic destructive inflammatory disease characterized by autoantibodies and the accumulation and persistence of an inflammatory infiltrate in the synovial membrane that leads to synovitis and the destruction of the joint architecture. The objective of this study was to evaluate the possible beneficial additional value of non-surgical periodontal therapy on systemic markers of inflammation and clinical and serological parameters of rheumatoid arthritis.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects affected by rheumatoid arthritis with a stable therapeutic regimen for at least 3 months preceding the study participation
  • Subjects with at least 15 teeth
  • Subjects affected by severe generalized periodontitis that had undergone no periodontal treatment in the 6 months preceding the study participation

Exclusion criteria

  • Age younger than 18 years
  • Pregnancy or breastfeeding
  • Edentulism
  • Diagnosis of other autoimmune pathologies, liver disease, diabetes, early/juvenile arthritis or syndromes associated with RA

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups

Immediate periodontal treatment
Experimental group
Description:
Subjects assigned to this group were receiving non-surgical periodontal treatment as well as oral hygiene instructions immediately after their inclusion. All subjects were undergone full periodontal and rheumatologic clinical examinations both at baseline and 90 days after the completion of the treatment. Blood collection for the analysis of the serum concentration of CRP, ESR, Fibrinogen, IL-6 and TNF-α was also performed at baseline and 90 days after periodontal treatment.
Treatment:
Procedure: Immediate non-surgical periodontal treatment and oral hygiene instructions
Delayed periodontal treatment
No Intervention group
Description:
Subjects assigned to this group were receiving non-surgical periodontal treatment 90 days after baseline evaluation. All subjects were undergone full periodontal and rheumatologic clinical examinations both at baseline and 90 days after. Blood collection for the analysis of the serum concentration of CRP, ESR, Fibrinogen, IL-6 and TNF-α was also performed at baseline and 90 days after.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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