A trial to examine the effect of intensive UA-lowering therapy in patients with CKD and hyperuricemia
- Conditions
- Patients with CKD and hyperuricemia
- Registration Number
- JPRN-UMIN000026741
- Lead Sponsor
- ara medical Univ
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 370
Not provided
Excluding criteria 1. History of hypersensitivity to topiroxostat 2. Being treated with either febuxostat or topiraxostat 3. History of repeated gouty arthritis attack 4. History of attacks of urinary stone within 6 months 5. Obstructive urinary tract disorders 6. Primary or secondary hyperuricemia (congenital myogenic hyperuricemia, hematopoietic tumor, solid tumor, secondary polycythemia, hemolytic anemia, tumor lysis syndrome, rhabdomyolysis, multiple sclerosis, multiple juvenile gout nephropathy, polycystic kidney etc.) 7. active malignancy 8. Severe hepatic dysfunctions (transaminase >= 100 IU / L) 9. Poorly controlled diabetes mellitus (HbA1c> 8.4%) 10. Severe hypertension (sBP >= 180 mm Hg or dBP >= 110 mm Hg) 11. Pregnant patients / lactating patients, female patients who wish to become pregnant during the study 12. Being or supposed to be under medication with mercaptopurine hydrate and azathioprine that are contraindicated with topiroxostat. 13. Any antihypertensive drugs have been changed within a month or will be changed after the trial registration 14. Currently participating in other intervention studies (no restrictions are applied to participation in other observational study) 15. Suffering acute illnesses that may affect the effectiveness and safety until the main registration after primary registration 16. The participation to this study is judged inappropriate by the attending physicianto
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method