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临床试验/NCT00532246
NCT00532246已完成4 期

A Study of Carotid Artery Intima-Media Thickness Following Exposure to Raloxifene HCl or Placebo

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 147 人开始时间: 2003年3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
147
试验地点
1
主要终点
Test the hypothesis that in postmenopausal women with osteoporosis who took lipid lowering meds for more than 6 months > 80% compliant with study drug during CORE trial, mean carotid IMT will be lower in patients treated with raloxifene than placebo

研究概览

简要总结

The purpose of this study is to measure carotid artery IMT at a single visit in a subset of women previously enrolled in the CORE (H3S-MC-GGJY) trial

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
55 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients must have completed the Eli Lilly and Company clinical trial CORE (H3S-MC-GGJY) inclusive of visit 5, in one of the 9 participating study sites in California.
  • Patients must have been dispensed study drug in the CORE trial (H3S-MC-GGJY).

排除标准

  • Have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
  • Have previously withdrawn from this exploratory study or any other study investigating raloxifene
  • Are employed by Eli Lilly and Company (that is, employees, temporary contract workers, or designees responsible for the conduct the study). Immediate family of Eli Lilly and Company employees may participate in Lilly-sponsored clinical trials, but are not permitted to participate at an Eli Lilly and Company facility. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted
  • Are investigator site personnel directly affiliated with the study, or are immediate family of investigator site personnel directly affiliated with the study. Immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted

研究组 & 干预措施

A

Experimental

raloxifene

干预措施: raloxifene (Drug)

B

Placebo Comparator

placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Test the hypothesis that in postmenopausal women with osteoporosis who took lipid lowering meds for more than 6 months > 80% compliant with study drug during CORE trial, mean carotid IMT will be lower in patients treated with raloxifene than placebo

次要结局

  • To test the hypothesis that, in postmenopausal women with osteoporosis, mean carotid IMT will be significantly lower in patients treated with raloxifene as compared to mean carotid IMT in patients treated with placebo in the following:
  • All enrolled patients who have not been exposed to lipid lowering medication for more than 6 months while in the CORE trial, regardless of study drug compliance.
  • All enrolled patients, regardless of lipid lowering drug exposure or compliance with study drug while in CORE
  • All enrolled patients who were at least 80% compliant with study drug while in CORE, regardless of use of lipid lowering therapy

研究者

申办方类型
Industry

研究点 (1)

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