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Gout and hyperuricemia clinical cohort

Gout and hyperuricemia clinical cohort project

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126489
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gout and hyperuricemia

Interventions

hyperuricemia:no
gout:no

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Met the 2015 American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) diagnostic criteria for gout; 2.Meets the diagnostic criteria for hyperuricemia, which means that adults with normal purine diet, regardless of gender, have fasting blood uric acid levels higher than 420 µ mol/L on non same day occasions. 3.Gender not limited, age = 8 years old; 4.Research participants are informed, voluntarily sign informed consent forms, and agree to follow up according to the requirements of queue data collection and undergo relevant examinations;

Exclusion criteria

Exclusion criteria: 1.Pregnant, pregnant or lactating women; 2.Individuals with mental illnesses who lack self-awareness and are unable to express themselves accurately; 3.Refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
ucic acid;—

Countries

China

Contacts

Public ContactZhu Xiaoxia

Huashan Hospital, Fudan University

15901811889@163.com+86 21 5288 7332

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026