Study on efficacy and safety of combination treatment with febuxostat and inosine for patients with heart failure
Not Applicable
- Conditions
- heart failure
- Registration Number
- JPRN-UMIN000025427
- Lead Sponsor
- Tsukuba International Clinical Pharmacology Clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 6
Inclusion Criteria
Not provided
Exclusion Criteria
1.Subject who has or had hypersensitivity, idiosyncracy (allergy) to drug. 2.Subjects taking azathioprine or mercaptopurine 3.Subject who has or had renal function disorder. 4.Subject with a history of gout, hyperuricemia or urolithiasis. 5.Patients who changed therapeutic drugs and treatment methods within 1 month before administration of test drugs 6.Subject who was judged not to be appropriate by the principal investigator or sub investigators by other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method