NCT00316641Unknown3 期
The Clinical Evaluation of Efficacy of Lipid-Lowing Tea on Hyperlipidemia Patients' Lipid Profiles
适应症
相关药物
试验速览
- 阶段
- 3 期
- 试验地点
- 2
研究概览
简要总结
The purpose of this study is to determine whether the Lipid-lowing Tea is effective and safe in the treatment of Hyperlipidemia Patients
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 盲法
- Double
入排标准
- 年龄范围
- 20 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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, β-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.
研究者
研究点 (2)
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