Hyperuricemia, Anserine, Pharmacokinetic Clinical Trial
NCT number | NCT00207974 |
Other study ID # | DMR94-IRB-68 |
Secondary ID | |
Status | Active, not recruiting |
Phase | Phase 1 |
First received | September 16, 2005 |
Last updated | November 16, 2005 |
Verified date | September 2005 |
Source | China Medical University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Department of Health |
Study type | Interventional |
Hyperuricemia is often associated with metabolic syndrome, which is a known precursor of atherosclerosis. The Yaizu Suisankagaku Industry Company have developed industrial production, named Marine Active. Human clinical trials showed reduction of creatine phosphokinase activity and sero-uric acid. Randomize, double blind clinical trial is entrust to our hospital. This study design is blood sampling from the health men who take 1 gm of marine active to analyse the pharmacokinetics of anserine.
Status | Active, not recruiting |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 20 Years to 35 Years |
Eligibility |
Inclusion Criteria: -Male volunteers, age between 20 to 35 years Exclusion Criteria: - Chronic medical history - Significant liver or renal dysfunction, - Have been administrated by any drug within 2 weeks before the initiation of study. |
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Taiwan | China Medical University Hospital | Taichung |
Lead Sponsor | Collaborator |
---|---|
China Medical University Hospital |
Taiwan,