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Search / Trial NCT05434858

Imagery as Biomarker of Gout

Launched by LILLE CATHOLIC UNIVERSITY · Jun 27, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Dual Energy Computed Tomography Hyperuricemia Gout Monosodium Urate Crystals

ClinConnect Summary

This clinical trial, titled "Imagery as Biomarker of Gout," is investigating whether certain deposits of crystals in the body, which can be seen using ultrasound or a special type of imaging called DECT, are linked to the development of gout in people with high uric acid levels. Gout is a painful condition that can occur when too much uric acid builds up in the body. The study will follow participants for five years to see if those with these crystal deposits develop symptoms of gout.

To participate in this study, individuals must be between 18 and 80 years old and have a high level of uric acid in their blood but should not currently have any symptoms of gout. Participants will undergo imaging tests to check for crystal deposits. It's important to note that individuals with certain serious health conditions, those who have previously had gout symptoms, or those currently taking specific medications for gout will not be eligible. This trial aims to better understand how crystal deposits relate to the onset of gout, which could help improve future prevention and treatment strategies.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Serum urate level ≥ 80 mg/L on inclusion,
  • No current or previous clinical symptoms of gout (including clinically apparent flares or tophus),
  • Between 18 and 80 years old,
  • Able to give informed consent.
  • Exclusion Criteria:
  • GFR (glomerular filtration rate) \<30 ml / min / 1.73 m² or dialysis,
  • Serious illness with a poor prognosis of less than 5 years,
  • Autoimmune inflammatory arthritis,
  • Change of geographical area within 5 years,
  • Previous analysis of synovial fluid showing crystals of MSU,
  • Presence of subcutaneous tophi,
  • Taking a hypouricaemic treatment (allopurinol, probenecid, benzbromarone, febuxostat, lesinurad), canakinumab, anakinra or colchicine,
  • Uricemia observed only after an acute decompensation of comorbidity
  • Pregnant or breastfeeding women

About Lille Catholic University

Lille Catholic University, a prominent academic institution in France, is dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on interdisciplinary collaboration, the university integrates expertise from various fields to foster the development of cutting-edge medical solutions. Its commitment to ethical standards and patient-centered approaches ensures that clinical trials conducted under its auspices are rigorous, scientifically sound, and aligned with the highest standards of care. By leveraging its extensive network of researchers, healthcare professionals, and resources, Lille Catholic University plays a vital role in contributing to the enhancement of medical knowledge and the improvement of patient outcomes.

Locations

Lille, Nord Pas De Calais, France

Patients applied

0 patients applied

Trial Officials

Tristan Pascart, MD, PhD

Principal Investigator

Lille Catholic University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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