Hyperlipidemia Clinical Trial
NCT number | NCT00316641 |
Other study ID # | DMR93-IRB-71 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 3 |
First received | April 20, 2006 |
Last updated | November 6, 2006 |
The purpose of this study is to determine whether the Lipid-lowing Tea is effective and safe in the treatment of Hyperlipidemia Patients
Status | Recruiting |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 20 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patient aged 20-65 years;either sex - Patient diagnosed with hyperlipidemia(fasting levels of TC>=200mg/dL),or TG>=200mg/dL but <400mg/dL,or LDL-C>=130mg/dL) - Patient who has signed the informed consent form Exclusion Criteria: - Patient with pregnancy (or child bearing potential),or in lactation - Patient with any lipid regulating agents within 4 weeks prior to study period - Patient currently taking concomitant medications, such as oral contraceptives, or any medical treatment capable of interfering with lipid metabolism(eg thiazides, ß-blockers, cyclosporins, itraconazole erythromycin,and danazol) - Patient with medical history of hypothyroidism, pancreatitis, cholestasis, nephrotic syndrome, gall bladder disease, primary biliary cirrhosis. - Patient with liver dysfunction (SGOT or SGPT>2x ULN) - Patient with renal insufficiency (serum creatinine>1.3mg/dL) - Patient with myocardial infarction,cerebrovascular disease,or major operations within 6 months prior to the study period. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind
Country | Name | City | State |
---|---|---|---|
Taiwan | China Medical University Hospital | Taichung |
Lead Sponsor | Collaborator |
---|---|
China Medical University Hospital |
Taiwan,
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