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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05522504
Other study ID # SHSY-IEC-4.1/21-246/01
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 15, 2022
Est. completion date February 2025

Study information

Verified date May 2024
Source Shanghai 10th People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate whether immune cells and their subtypes in peripheral blood affects the asymptomatic hyperuricemia, gout flare, intercritical gout and advanced gout.


Description:

A number of studies have reported that innate immunity cells (such as blood monocytes and neutrophils) play a crucial role in the initiation and amplification of gout flare resulted from MSU deposition in the joint or tissue, leading to release NLRP3 inflammasome-mediated production of bioactive IL-1β. Further investigation demonstrated the role of blood neutrophils might contribute to the resolution of gout flare by forming aggregated neutrophil extracellular traps. Recently, a few in vitro experiments have indicated that adaptive immunity may be involved in mechanisms of gout. However, a global understanding of blood immune responses underlying gout is still unclear. Thus, we want to investigate the relationship between immune cells and their subtypes in peripheral blood and the gout.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 600
Est. completion date February 2025
Est. primary completion date February 15, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - gout flare:diagnosis with gout flare at this hospital according to the criteria approved by the ACR Board of Directors and the EULAR Executive Committee in 2015 - intercritical gout: remission of gout patients were classified into intercritical gout group without tophi, chronic gouty arthritis, or imaging erosion(All of these gout remission patients underwent dual-energy CT test within one month, and were detected to have MSU crystal deposition in local joints) - advanced gout: gout remission patients were classified into advanced gout group characterized by tophi, chronic gouty arthritis, or imaging erosion(All of these gout remission patients underwent dual-energy CT test within one month, and were detected to have MSU crystal deposition in local joints) - asymptomatic hyperuricemia: hyperuricemia in men was defined as SUA = 420 mmol/L without any complications Exclusion Criteria: - primary osteoarticular diseases - unwilling participation in the study - corticosteroids or indomethacin use in the past 3 months; - septic arthritis or another joint disease (such as rheumatoid arthritis); - impaired renal function (creatinine clearance <30 mL/min) and other conditions which may increase the level of blood uric acid

Study Design


Locations

Country Name City State
China Department of Nephrology & Rheumatology, Shanghai Tenth People's Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Ai Peng

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary remission of gout Patients fulfilling all the domains of the 2016 preliminary remission criteria for gout were defined as gout remission group 6 month
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