CTRI/2011/04/001689已完成3 期
A randomized, open label, phase III, comparative, multicentric study to assess the efficacy and safety of Fenofibric acid delayed release capsules versus Fenofibrate tablets in patients with dyslipidemia
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Patients with hypertriglyceridemia at the time of enrollment
- •2.Informed consent
排除标准
- •1.Pregnancy, lactation and women of childbearing potential not using appropriate contraceptive measures.
- •2.Patients already receiving drugs belonging to the fibric acid derivatives.
- •3.Patients with hepatic or renal dysfunction.
- •4.Patients with history of myopathy or evidence of active muscle disease.
- •5.Patients with any other serious concurrent illness or malignancy.
- •6.Patients with continuing history of alcohol and / or drug abuse.
- •7.Patients with persistent gall bladder diseases.
- •8.Patients with known hypersensitivity to fenofibric acid.
- •9.Participation in another clinical trial in the past 3 months
研究者
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