hyperuricemia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Japanese healthy volunteers who are 20 years or older and younger than 50
Exclusion criteria
Exclusion criteria: 1.Disease that should be treated 2. On medical treatment 3. Hepatic dysfunction(AST>40 IU/L or ALT>40 IU/L) 4. Renal dysfunction (serum creatinine level>1.2 mg/dL) 5. History of cardiovascular disease 6. Serum uric acid level >7.5 mg/dL 7. Abnormal electrolytes values (Na or K) 8. Hematocrit >55 % 9. Allergy reaction to thiazide and its related diuretics 10. Woman who is pregnant or breastfeeding 11. Systolic blood pressure <90 mmHg or >140 mmHg (sitting position) 12. Body weight <40 kg or >90 kg 13. Not appropriate to this study by other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Relation between MRP4 genotype and the changes of serum uric acid levels and uric acid clearance after multiple administration of trichlormethiazide | — |
Secondary
| Measure | Time frame |
|---|---|
| Change of serum electrolytes, cholesterol, triglycerides, pulse rate and blood pressure Ratio of side effects by trichlormethiazide | — |
Countries
Japan
Contacts
Faculty of Medical Sciences, Kyushu University Department of Clinical Pharmacology