Synovial Fluid Bank From Arthritic Patients

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2007 by Universitaire de Sherbrooke.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Canadian Arthritis Network
Information provided by:
Universitaire de Sherbrooke
ClinicalTrials.gov Identifier:
NCT00512343
First received: August 3, 2007
Last updated: NA
Last verified: August 2007
History: No changes posted
  Purpose

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


Condition
Arthritis

Study Type: Observational
Study Design: Observational Model: Defined Population
Primary Purpose: Screening
Time Perspective: Cross-Sectional
Time Perspective: Retrospective/Prospective
Official Title: Establishment of a Bank of Synovial Fluids and Paired Sera From Arthritic Patients for the Evaluation of New Methods Facilitating the Diagnosis and the Monitoring of Progression and Therapy of Arthritis.

Further study details as provided by Universitaire de Sherbrooke:

Estimated Enrollment: 300
Study Start Date: June 2002
Estimated Study Completion Date: September 2009
Detailed Description:

Our group has developped 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 pre-clinical studies to evaluate, alone or by combination testings, the potential of novel biomarkers for their prevalence and diagnostic/prognotic 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. 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.

  Eligibility

Ages Eligible for Study:   3 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

- Significant joint effusion

Exclusion Criteria:

  • Hemorragic effusion
  • Traumatic effusion
  • Less than 3 ml total of collected fluid (used for routine analysis and culture)
  • Inability or refusal to consent
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00512343

Contacts
Contact: Gilles Boire, MD, MSc (819) 564-5261 Gilles.Boire@USherbrooke.ca

Locations
Canada, Quebec
Centre hospitalier universitaire de Sherbrooke Recruiting
Sherbrooke, Quebec, Canada, J1H 5N4
Contact: Gilles Boire, MD, MSc     (819) 564-5261     Gilles.Boire@USherbrooke.ca    
Principal Investigator: Gilles Boire, MD, MSc            
Sponsors and Collaborators
Universitaire de Sherbrooke
Canadian Arthritis Network
Investigators
Principal Investigator: Gilles Boire, MD, MSc CHUS and Université de Sherbrooke
  More Information

Publications:
ClinicalTrials.gov Identifier: NCT00512343     History of Changes
Other Study ID Numbers: 02-12 LS, 91597
Study First Received: August 3, 2007
Last Updated: August 3, 2007
Health Authority: Canada: Ethics Review Committee

Keywords provided by Universitaire de Sherbrooke:
Synovial Fluid
Arthritis
Paired serum/synovial fluid samples

Additional relevant MeSH terms:
Arthritis
Joint Diseases
Musculoskeletal Diseases

ClinicalTrials.gov processed this record on May 23, 2013