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Evaluation of efficacy of urinary uric acid excretion and urolithiasis related factor in urolithiasis patients with hyperuricemia by combination therapies of "Feburic tablets" and "Uralyt".

Evaluation of efficacy of urinary uric acid excretion and urolithiasis related factor in urolithiasis patients with hyperuricemia by combination therapies of "Feburic tablets" and "Uralyt". - Evaluation of efficacy of urinary uric acid excretion and urolithiasis related factor in urolithiasis patients with hyperuricemia by combination therapies of "Feburic tablets" and "Uralyt".

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008752
Enrollment
40
Registered
2012-08-23
Start date
2012-08-23
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Urolithiasis patients with hyperuricemia

Interventions

Feburic tablets Uralyt Feburic tablets and Uralyt No medication

Sponsors

Kanazawa Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) More than 20 years old Japanese male patient age at the time of obtaining informed consent. 2) Patients with serum uric acid level are greater than 7.0mg/dl. 3) Patient in the previous two weeks, not taking uric acid-lowering drugs. 4) Informed consent.

Exclusion criteria

Exclusion criteria: 1) The patient who is developing gouty arthritis at the time of an eligibility judging, or has not passed two weeks since a gout arthritis disappearance day. 2) The patient who has not passed two weeks since the last medication day of the following combined use prohibition medicine at the time of an eligibility judging. Combined use prohibition drug of "Febric tablets". Mercaptopurine hydrate Azathioprine Combined use prohibition drug of "Uralyt". Hexamine mandelate 3) Serum creatinine level is more than 1.5 mg/dl. 4) Liver disease patients (either AST or ALT exceeds the twice of a standard value maximum). 5) Patients with severe cardiac disease, renal failure and other critical diseases. 6) Patients with drug allergy. 7) Patients who are considered to be inappropriate by the investigators.

Design outcomes

Primary

MeasureTime frame
Change of the clinical laboratory test result in four weeks of study, and the degree of super saturation of a calcium oxalate or calcium phosphate.

Countries

Japan

Contacts

Public ContactKatsuhito Miyazawa

Kanazawa Medical University Urology

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026