Clinical trial Recruiting at 1 site Observational Ages 18 and up

Observing crystal-related arthritis conditions

Official title: Data Collection for the Constitution of an Observatory for Patients Suffering From Microcrystalline Rheumatism With Morphological Phenotyping

Run by Lille Catholic University · NCT04695028 · Data updated 2026-11-12

This study is trying to learn more about conditions like gout and chondrocalcinosis by collecting information from patients and using imaging tests to see how these diseases change over time.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1000 (estimated)
SponsorLille Catholic University
Academic / other
Locations1 site (Lomme)
StatusRecruiting
StartedMarch 16, 2021
Main results expectedOctober 2023
Study endsOctober 2030
Registry record updatedJune 23, 2023
Trial IDNCT04695028 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals diagnosed with gout, calcium pyrophosphate dihydrate crystal deposition disease, or hydroxyapatite crystal rheumatism who require imaging.

Probably not a fit

Patients who refuse imaging procedures or oppose the use of their health data for research will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research aims to create an observatory for microcrystalline rheumatism, focusing on conditions like gout and chondrocalcinosis, at the Groupement des Hôpitaux de l'Institut Catholique de Lille. Patients already enrolled in a previous observational study will be included, along with new patients recruited during rheumatology consultations. Data on sociodemographic and clinical characteristics will be collected, and participants may undergo ultrasound and dual energy scanning for imaging. The study will track clinical and biological evolution over time to enhance understanding and management of these conditions.

Why it matters

Potential benefit: If successful, this study could lead to improved diagnosis and management of crystal-related arthropathies for patients.

How similar studies have gone: Other studies have shown success in using imaging techniques to better understand and manage similar conditions, indicating a promising approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosis of gout according to American College of Rheumatology /European League Against Rheumatism (ACR/EULAR) 2015 criteria OR diagnosis of calcium pyrophosphate dihydrate crystal deposition disease (CPPD) based on EULAR 2011 recommendations OR diagnosis of hydroxyapatite crystal rheumatism (HCR) according to a typical clinical sequence and demonstration of compatible calcium deposits on imaging
* patient who will benefit or has benefited from an ultrasound and/or DECT evaluation of microcrystalline deposits
* clinical suspicion of microcrystalline rheumatism requiring further imaging to confirm the diagnosis

Exclusion Criteria:

* Refusal or contra-indication to perform ultrasound or dual energy scanning.
* Patient's opposition to the use of his or her health data for research purposes
* Patient under guardianship or curatorship
* Pregnant woman
* Person not affiliated to a social security scheme or entitled to a social security benefit

Where it's running

  • GHICL- Hôpital Saint Philibert
    Lomme, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.