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临床试验/EUCTR2005-000807-33-SE
EUCTR2005-000807-33-SE进行中(未招募)不适用

Randomized, double-blind, two -arms placebo-controlled, parallel-group, multicenter study of rimonabant 20 mg once daily in the treatment of atherogenic dyslipidemia in abdominally obese patients. - ADAGIO-Lipids

sanofi-aventis recherche & développement0 个研究点目标入组 740 人开始时间: 2005年4月7日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
740

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Male or female patients aged =18 years
  • Waist circumference > 102 cm in men and > 88 cm in women
  • Dyslipidemia consisting of:
  • - Triglyceridemia = 1.50g/L (i.e. 1.69mmol/L) and = 7.0g/L (i.e. 7.90mmol/L)
  • - HDL cholesterol < 50mg/dL (1.29mmol/L) in women and < 40mg/dL (1.04mmol/L)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Weight change > 5 kg within 3 months prior to screening visit
  • Pregnancy or lactation, or women planning to become pregnant
  • Absence of medically approved contraceptive methods for females of childbearing
  • Marijuana or hashish users
  • Presence of any other condition (e.g. geographic, social…) actual or anticipated, that
  • the Investigator feels that would restrict or limit the subject’s participation for the
  • duration of the study.

研究者

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