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临床试验/NCT01081548
NCT01081548已完成4 期

A Multi-center, Randomized, Open-labeled Clinical Trial to Evaluate Efficacy and Safety of Lipinon® 20mg Versus Lipitor® 20mg in Korean Patients With Hypercholesterolemia

Yonsei University1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2008年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
17
试验地点
1

研究概览

简要总结

The purpose of this study is to compare the efficacy and safety of atorvastatin generic product with reference drug.

研究设计

研究类型
Interventional
干预模型
Parallel
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Age 20 ~ 79
  • People who have not reached LDL-C targeted level in accordance with the guidelines for hyperlipidemia management released by Korean Society of Lipidology and Atherosclerosis
  • In case of female participants taking combination HRT or oral contraceptive, they should maintain stable capacity and usage at least for 8 weeks before the visit 1.

排除标准

  • 未提供

研究组 & 干预措施

Generic

Experimental

干预措施: atorvastatin (Drug)

Lipitor

Active Comparator

干预措施: atorvastatin (Drug)

研究者

申办方类型
Other

研究点 (1)

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