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临床试验/ACTRN12605000777695
ACTRN12605000777695尚未招募3 期

A multicenter, double-blind, randomized study to compare the efficacy and safety of the combination of 145mg fenofibrate and simvastatin with 40mg simvastatin monotherapy in patients with mixed dyslipidemia at risk of cardiovascular disease not adequately controlled by 40 mg simvastatin alone

Fournier Laboratories Ireland0 个研究点目标入组 400 人开始时间: 2005年12月7日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
ot stated 至 ot stated(—)
性别
All

入选标准

  • Patients with mixed dyslipidemia with CHD or CHD risk equivalent or with multiple risk factor and a 10 year risk above or equal to 10% and with TG above 1.71mmol/l and LDL >2.58 or >3.36mmol/l according to risk after 6 weeks of treatment with 40mg simvastatin.

排除标准

  • Diabetes, CK>2 times ULN, creatinine clearance > 80ml/min, LFTs >2 times ULN.

研究者

发起方
Fournier Laboratories Ireland

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