Rare Disease Trial, Recruiting NCT07302074 Sponsor: University Hospital, Brest Condition: Rare Disease
Back to Rare Disease

Rare Disease Trial, Recruiting

NCT07302074
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have signed a consent form agreeing to take part
  • You are 18 years old or older
  • You are covered by a social security (health insurance) scheme
  • (For the "cases" group) You have been referred for joint inflammation (arthritis) or inflammation of a fluid-filled sac near a joint (bursitis) linked to a rare autoimmune disease or a side effect of medication, confirmed by ultrasound scan
  • (For the "control" group – arthritis) You have joint inflammation confirmed by ultrasound, and you have been diagnosed with rheumatoid arthritis, a form of spondyloarthritis, psoriatic arthritis, or reactive arthritis according to recognised medical criteria
  • (For the "control" group – bursitis) You have inflammation of a fluid-filled sac near a joint confirmed by ultrasound, and you meet the recognised criteria for a condition called polymyalgia rheumatica

Who may not be able to join:

  • You are under a legal protection order or are unable to give your own consent
  • You are pregnant or currently breastfeeding
  • You are taking blood-thinning medications such as warfarin (Coumadin), fluindione, apixaban (Eliquis), dabigatran (Pradaxa), rivaroxaban, or heparin at treatment doses
  • There is a reason you cannot safely have a local procedure on the joint, such as swelling caused by lymph drainage problems near the joint, an open wound at the joint site, an artificial joint replacement at the affected joint, or a steroid injection into the same joint within the last 3 months
  • You have been treated with a type of medication called a biologic therapy or a JAK inhibitor in the last 3 months, or with a medication called Rituximab in the last 6 months

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +33(0)298347264

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital, Brest
Registry
ClinicalTrials.gov
Start date
27 March 2026
Est. completion
3 March 2031

Where this trial is recruiting

🇫🇷 France

Primary endpoints

characterize the inflammatory infiltrate in synovial biopsies

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov