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Study for the effectiveness of different courses of low-dose colchicine for preventing acute flares during urate lowering therapy by febuxostat

Study for the effectiveness of different courses of low-dose colchicine for preventing acute flares during urate lowering therapy by febuxostat

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020315
Enrollment
Unknown
Registered
2018-12-23
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Gout

Interventions

1:4 weeks of low-dose colchicine for preventing
2:12 weeks of low-dose colchicine for preventing
3:24 weeks of low-dose colchicine for preventing

Sponsors

The Second Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18 to 75 years old male or female; 2) Meet the diagnostic criteria for primary gout; 3) Acute flare within 1 month, without urate lowering therapy, serum uric acid >420umol/L.

Exclusion criteria

Exclusion criteria: 1) Those who are allergic to all the drugs or ingredients in this test, or those who are allergic to the disease, or those with high sensitivity; 2) Azorazin, 6-mercaptopurine, cyclosporine, cyclophosphamide, pyrazinamide, sulfamethoxazole, trimethoprim, theophylline, warfarin or other coumarins are currently or need a drug such as a coagulant; 3) patients with active peptic ulcer, malignant tumors, and active tuberculosis; 4) Arthritis caused by other causes has been diagnosed; 5) heart failure, unstable heart pain, history of myocardial infarction or other serious heart disease in the past 12 months; 6) Patients with secondary hyperuricemia caused by blood diseases, malignant tumors, kidney diseases or tumor radiotherapy and chemotherapy; 7) Patients with active liver disease or cirrhosis, or abnormal liver function (serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) exceeds the upper limit of the normal range by 2.5 times; 8) white blood cell count <4.0 × 10^9/L, or platelets <100×10^9/L, or hemoglobin <90g/l; 9) Brain diseases, abnormal judgment ability, and mental disorders cannot cooperate; 10) History of alcohol abuse or illegal drugs; 11) Pregnant women, pregnant or lactating women; 12) For any other reason, the investigator believes that it is inappropriate to participate in the tester.

Design outcomes

Primary

MeasureTime frame
total times of flare;

Secondary

MeasureTime frame
flare times in 4/12/24 weeks;target serum uric acid level achievement rate;tophus volume change in tophaeous gout;vas score of flares,peak time,duration;dosage of NSAIDs of prednisone;rate of abnormal liver function;

Countries

China

Contacts

Public ContactWu Huaxiang

The Second Affiliated Hospital, Zhejiang University School of Medicine

wuhx8855@sina.com+86 0571 89713751

Outcome results

None listed

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