Gout
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who have completed the Phase I clinical trial evaluating the safety and pharmacokinetic characteristics of recombinant human interleukin-1 receptor antagonists for injection in patients with gouty arthritis in the intermittent phase or the multicenter Phase IIa clinical trial evaluating the safety and efficacy of UA007 in patients with acute attacks of gouty arthritis at our center; 2. During the participation in clinical trials, the informed consent form for biological samples and health-related information donors has been signed.
Exclusion criteria
Exclusion criteria: The sample is not suitable for testing, including sample contamination, sample hemolysis, insufficient sample size, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| asymmetric dimethylarginine;endothelin-1;malondialdehyde;protein carbonyls,PCO;nitro tyrosine;vascular cell adhesion molecule-1;intercellular cell adhesion molecule-1;E-Selectin;IL-1ß;IL-6;IL-8;IL-18;proteomic analysis; | — |
Countries
China
Contacts
Zhongshan Hospital,Fudan University