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临床试验/NCT00885612
NCT00885612已完成不适用

10-year CHD Risk Evaluation and Its Treatment Pattern Analysis in Postmenopausal Early Breast Cancer Patients Taking Aromatase Inhibitors

AstraZeneca1 个研究点 分布在 1 个国家目标入组 1,114 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
1,114
试验地点
1
主要终点
The primary objective of this study is to define 10-year CHD risk according to Framingham risk score in postmenopausal early breast cancer patients who are taking aromatase inhibitors as an adjuvant treatment.

研究概览

简要总结

10-year CHD risk evaluation and its treatment pattern analysis in postmenopausal early breast cancer patients taking aromatase inhibitors.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

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

入选标准

  • Early Breast Cancer patients
  • Postmenopausal Status
  • patients taking Aromatase Inhibitor as adjuvant treatment no longer than 6 months

排除标准

  • Advanced Breast Cancer patients(stage iii, iv)
  • Patients who are hard to be analysed by limitation of chart record according to investigators discretion
  • patients who already have been registered in this study

结局指标

主要结局

The primary objective of this study is to define 10-year CHD risk according to Framingham risk score in postmenopausal early breast cancer patients who are taking aromatase inhibitors as an adjuvant treatment.

时间窗: 1 visit

次要结局

  • To describe 10-year CHD risk comparing to the historical data of 10-year cancer-specific mortality in breast cancer(1 Visit)
  • To analyse CHD management patterns according to defined 10-year CHD risk categories(1 Visit)
  • To describe correlation between concommitant medication(Anthracycline, Trasuzumab) and CHD risk(1 Visit)

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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