Hyperuricemia Clinical Trial
Official title:
Use of Febuxostat in Hyperuricemia Among Hemodialysis Patients
Verified date | May 2017 |
Source | Benha University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hyperuricemia is not infrequently encountered among hemodialysis patients. However, there is no clear data about use of febuxostat among hemodialysis patients, apart from very small case series. The aim of this study is to investigate the efficacy of using febuxostat for the treatment of Hyperuricemia among hemodialysis patients.
Status | Completed |
Enrollment | 19 |
Est. completion date | May 1, 2017 |
Est. primary completion date | April 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - Age above 18 years - Hemodialysis patient - Hyperuricemia (Uric acid level above 6.0 mg/dL in females and 7.0 mg/dL in males) Exclusion Criteria: - Patient currently and/or recently received drugs for hyperuricemia within the last three months - Patient had recent (within 3 months) change of erythropoiesis stimulating drugs or other drug known to increase uric acid e.g furosemide |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Benha University | New Jeddah Clinic Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in serum uric acid | Change in serum uric acid after 3 months of Febuxostat 40 milligrams Tablet therapy | at three months of Febuxostat 40 milligrams Tablet therapy |
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