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Time Required to Dissolve Urate Deposits in Patients With Gout

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test, Biological
Study Type: Observational
SUMMARY

Gout is characterized by episodes of acute arthritis of the lower limbs due to intermittent activation of innate immunity in the joints where urate crystals have formed. These crystals occur when serum urate (SUA) levels have been above 70 mg/L for many years. They can be dissolved by lowering SUA levels to at least 60 mg/L (treat-to-target - T2T - strategy). Once the crystals are dissolved, patients are no longer symptomatic and are considered to be in remission (treat-to-dissolve - T2D - strategy). The presence of crystals and their dissolution during treatment can be monitored by repeated ultrasound (US) scans of the feet and knees. The time required for complete dissolution varies from patient to patient. ReViGore40 is a cohort designed to i) determine the time to complete dissolution of urate deposits in joints when SUA levels are maintained below 40 mg/L, ii) determine the factors (clinical, biological, genetic) associated with the time required for complete dissolution of urate deposits within joints.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age over 18 years

• Gout according to the ACR/Eular 2015 criteria

• SUA levels greater than 60 mg/L

• US score (MTP1s, knees) ≥2/24

• Informed consent Dated and signed voluntarily

Locations
Other Locations
France
APHP, Lariboisière Hospital, Rheumatology departement
RECRUITING
Paris
Contact Information
Primary
Pascal RICHETTE, PR
pascal.richette@aphp.fr
0149956314
Time Frame
Start Date: 2024-09-24
Estimated Completion Date: 2032-09-24
Participants
Target number of participants: 250
Treatments
Gout patients treated according to a Treat-to-Dissolve strategy
Patients initiated with ULT (urate target less than 40 mg/L), and followed every 6 months with Ultrasound until complete urate dissolution
Related Therapeutic Areas
Sponsors
Collaborators: Institut National de la Santé Et de la Recherche Médicale, France, ART VIGGO Association for Research
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov