NCT00512343

Brief 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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
53mo left

Started Jun 2002

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress85%
Jun 2002Sep 2030

Study Start

First participant enrolled

June 1, 2002

Completed
5.2 years until next milestone

First Submitted

Initial submission to the registry

August 3, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 7, 2007

Completed
20.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2027

Expected
2.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2030

Last Updated

March 25, 2025

Status Verified

March 1, 2025

Enrollment Period

25.5 years

First QC Date

August 3, 2007

Last Update Submit

March 24, 2025

Conditions

Keywords

Synovial FluidArthritisPaired serum/synovial fluid samples

Outcome Measures

Primary Outcomes (1)

  • Availability of paired synovial fluid and serum samples for exploratory studies

    Availability of paired synovial fluid and serum samples, linked with anonymized clinical and treatment data, from patients suffering from various arthritides (rheumatoid arthritis, gout and other microcrystalline arthritides, osteoarthritis, spondylarthropathies, juvenile idiopathic arthritis, and various other diseases, including inflammatory polyarthritis of recent-onset in adults

    Use with various collaborators at different times, upon request and approbation

Eligibility Criteria

Age3 Years - 95 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients suffering from various arthritides (rheumatoid arthritis, gout and other microcristalline arthritides, osteoarthritis, spondylarthropathies, juvenile idiopathic arthritis, and various other diseases, including inflammatory polyarthritis of recent-onset in adults

You may qualify if:

  • Significant joint effusion

You may not qualify if:

  • Hemorrhagic effusion
  • Traumatic effusion
  • Less than 3 ml total of collected fluid (used for routine analysis and culture)
  • Inability or refusal to consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre hospitalier universitaire de Sherbrooke

Sherbrooke, Quebec, J1H 5N4, Canada

RECRUITING

Related Publications (2)

  • Kilani RT, Maksymowych WP, Aitken A, Boire G, St-Pierre Y, Li Y, Ghahary A. Detection of high levels of 2 specific isoforms of 14-3-3 proteins in synovial fluid from patients with joint inflammation. J Rheumatol. 2007 Aug;34(8):1650-7. Epub 2007 Jul 1.

  • Simard N, Boire G, de Brum-Fernandes AJ, St-Pierre Y. A novel approach to measure the contribution of matrix metalloproteinase in the overall net proteolytic activity present in synovial fluids of patients with arthritis. Arthritis Res Ther. 2006;8(4):R125. doi: 10.1186/ar2014.

Biospecimen

Retention: SAMPLES WITHOUT DNA

Synovial fluids from joints with effusion Sereum samples drawn on the same day

MeSH Terms

Conditions

Arthritis

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Study Officials

  • Gilles Boire, MD, MSc

    CHUS and Université de Sherbrooke

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Gilles Boire, MD, MSc

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

August 3, 2007

First Posted

August 7, 2007

Study Start

June 1, 2002

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

September 1, 2030

Last Updated

March 25, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Locations