跳至主要内容
临床试验/NCT00500734
NCT00500734Unknown不适用

Cardiomyopathy Tissue Bank in a Cancer Population

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2002年12月10日最近更新:
适应症

试验速览

阶段
不适用
入组人数
1,000
试验地点
1
主要终点
Identification biological markers predisposing cancer patients to development of chemotherapy-induced congestive heart failure

研究概览

简要总结

Any time the words "you," "your," "I," or "me" appear, it is meant to apply to the potential participant.

The goal of this laboratory research study is to collect and store blood and tissue from patients who have a diagnosis of heart disease and may be at a high risk for the development of heart failure. This blood may be used in the future to identify genes that may play a role in developing congestive heart failure (CHF) from chemotherapy or other sources.

This is an investigational study. All will be enrolled at MD Anderson.

详细描述

You will have a one time blood draw of 2 teaspoons of blood for use in future research. This blood may be studied in the future to try to find possible genetic or biochemical markers that may be the cause of CHF. Your blood will be drawn either on an outpatient basis or during a routine visit to the hospital. If you already have a central line or an IV placed, the blood will be drawn at these sites to decrease the pain and discomfort of the blood draw. The information obtained in this study will not be put into your medical records.

研究设计

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

入排标准

年龄范围
2 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are at high risk for developing Cardiomyopathy or Congestive Heart Failure.
  • Patients two months of age and older.

排除标准

  • Those that are not willing to sign an informed consent.

结局指标

主要结局

Identification biological markers predisposing cancer patients to development of chemotherapy-induced congestive heart failure

时间窗: One time visit for collection of blood and tissue samples.

Baseline Patient Demographic Information (age, sex, race)

时间窗: One time visit.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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