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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01156155
Other study ID # 0342-10-FB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 14, 2010
Est. completion date August 30, 2018

Study information

Verified date October 2023
Source University of Nebraska
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Periodontitis (PD) has been postulated to be a risk factor for the onset and progression of rheumatoid arthritis (RA). Recent reports suggest that infection with Porphyromonas gingivalis (P. gingivalis), a major oral pathogen in PD, could play a pivotal role in the development RA. The objective of this study is to examine the relationship of PD and P. gingivalis infection with the risk and severity of RA.


Description:

In this study, we will examine whether periodontitis (PD) and P. gingivalis impact rheumatoid arthritis (RA) risk by enrolling 300 patients with RA and 300 comparator patients with osteoarthritis and comparing results from comprehensive dental examinations and antibody responses to P. gingivalis. We will examine whether these associations are modified by the presence of certain genetic risk factors previously implicated in RA and whether evidence of infection with P. gingivalis precedes RA onset by examining banked sera from the Department of Defense Serum Repository (DoDSR) and the Studies of the Etiology of RA (SERA). We also plan to explore whether there are novel proteins expressed by P. gingivalis that drive autoimmunity in RA and whether immune responses to these bacterial proteins predict the future development of RA.


Recruitment information / eligibility

Status Completed
Enrollment 617
Est. completion date August 30, 2018
Est. primary completion date August 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Age 19 years or older - Diagnosis of rheumatoid arthritis, or osteoarthritis - Have 9 or more evaluable posterior teeth (out of a total of 28 teeth, excluding third molars) - Willing and able to provide informed consent Exclusion Criteria: - Received tetracyclines within the last 6 months. - Need for antibiotic premedication for dental probing. - Pregnant or breast feeding

Study Design


Intervention

Radiation:
Digital xray of jaw and teeth
one time xray of jaw and teeth
Procedure:
Blood draw
Three to four tablespoons of blood drawn.
Other:
questionnaires
completed questionnaires regarding patient's health and functional ability.
Procedure:
Periodontal Examination
Periodontal examination including measurement of gum pockets with a probe. Bacterial samples taken.
Other:
Bilateral digital xray of hands
One time digital xray of hands

Locations

Country Name City State
United States Veterans Affairs Medical Center, Omaha Omaha Nebraska

Sponsors (4)

Lead Sponsor Collaborator
University of Nebraska Dallas VA Medical Center, VA Salt Lake City Health Care System, Washington D.C. Veterans Affairs Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Show the associations of periodontitis with RA are primarily due to infection with P. gingivalis Clinically defined PD will be more common in RA patients than in controls. 1.B.: Clinically defined PD will be associated with greater RA disease severity including autoantibody status and the presence and extent of radiographic disease progression.
1.C.: The associations of clinically defined PD with RA risk and severity will be explained by the presence of antibody to P. gingivalis.
within thirty days of enrollment
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