Synovial Fluid Bank From Arthritic Patients

Last updated: March 24, 2025
Sponsor: Gilles Boire
Overall Status: Active - Recruiting

Phase

N/A

Condition

Joint Injuries

Treatment

N/A

Clinical Study ID

NCT00512343
02-12 LS
  • Ages 3-95
  • All Genders

Study Summary

The objectives of this group project is to collect synovial fluid (SF) and paired sera and carry out preclinical studies to evaluate, alone or by combination testings, the potential of novel biomarkers for their prevalence and diagnostic/prognostic values in patients with arthritis, and to determine how therapeutic intervention regulate their levels.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Significant joint effusion

Exclusion

Exclusion Criteria:

  • Hemorrhagic effusion

  • Traumatic effusion

  • Less than 3 ml total of collected fluid (used for routine analysis and culture)

  • Inability or refusal to consent

Study Design

Total Participants: 500
Study Start date:
June 01, 2002
Estimated Completion Date:
September 30, 2030

Study Description

Our group has developed interdisciplinary expertise in biomarkers related to distinct aspects of inflammation-induced joint damage, most notably those associated with degradation of components of the extracellular matrix, bone loss, or associated with post-translational changes on protease inhibitors.

The objectives of this group project is to collect SF and paired sera and carry out preclinical studies to evaluate, alone or by combination testings, the potential of novel biomarkers for their prevalence and diagnostic/prognostic values in patients with arthritis, and to determine how therapeutic intervention regulate their levels.

More specifically, we will study (1) biomarkers associated with osteoclastic bone resorption and synthesis/degradation of cartilage, (2) inhibitors of enzymes (calpastatin) that are preferentially targeted by rheumatoid patients, as well as (3) enzymes (e.g. Matrix Metalloproteinases (MMPs)) responsible for the cleavage of components of the articular cartilage.

Finally, we propose to characterize the repertoire of specific active proteases in the SF of arthritic patients concomitantly to the use biomarkers (neoepitopes of cleaved collagens) previously associated with cartilage destruction and synthesis to identify new targets for the development of protease inhibitors for the treatment of arthritis. Furthermore, our project will also provide the opportunity to test the potential of measuring the net proteolytic activity by Fluorescent-Activated Substrate Conversion as a method of monitoring disease activity and treatment efficiency in a clinical setting.

Connect with a study center

  • Centre hospitalier universitaire de Sherbrooke

    Sherbrooke, Quebec J1H 5N4
    Canada

    Active - Recruiting

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