Skip to content

Follow-up study for the curative effect of uric acid-reducing treatment in patients with hyperuricemia

Follow-up study for the curative effect of uric acid-reducing treatment in patients with hyperuricemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028684
Enrollment
Unknown
Registered
2019-12-30
Start date
2022-03-01
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

hyperuricemia

Interventions

promoting drug (benclomarone):Treatment with benzbromarone
suppressing synthetic drugs (febustat ):Treatment with febuxostat
suppressing synthetic drugs (allopurinol):Treatment with allopurinol

Sponsors

Shanghai Tenth People's Hospital affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old, male; 2. did not use uric acid lowering drugs before enrollment; 3. It is expected that the drug will be used for more than one year after enrollment; 4. Have complete baseline data; 5. in line with low purine diet; 6. There was no history of stress events such as infection and trauma in the past two weeks before enrollment.

Exclusion criteria

Exclusion criteria: 1. Have a history of any malignant tumor in the past 5 years; 2. People with active liver disease or abnormal liver function (ALT, AST, TBIL are more than 3 times the upper limit of normal values); or have a history of liver cirrhosis, decompensated stage of liver cirrhosis, or a history of liver encephalopathy; 3. Severe kidney disease; 4. Acute and chronic inflammatory lesions.

Design outcomes

Primary

MeasureTime frame
Blood biochemical tests;

Secondary

MeasureTime frame
ultrasound;Urine biochemical test;

Countries

China

Contacts

Public ContactHaibing Chen

Shanghai Tenth People's Hospital affiliated to Tongji University

18930173813@163.com+86 189 3017 3813

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026