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临床试验/NCT02442011
NCT02442011招募中不适用

Hematology Biobank: In Vitro Study of Blood Disorders

Albert Einstein College of Medicine1 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2014年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
2,000
试验地点
1
主要终点
Biobank

研究概览

简要总结

This is a biorepository of blood specimens from subjects with different Hematological disorders.

详细描述

There has been a marked increase in our knowledge of Blood Disorders in the last decade. Much of this knowledge comes from examining blood specimens from patients and subjecting these samples to red cell, plasma, serum or DNA analyses. The study team proposes to set up a Hematology biobank, which will include patient histories, their medical progress and a linked but de-identified bank of blood samples. This will enable researchers to have a large database, which can be used to learn more about these diseases.

The Hematology biobank will use whole blood, red blood cells, plasma, serum and/or DNA. Whole blood specimens, which by definition include the white cells that contain DNA, will be collected and stored in the biobank repository at the Institute for Clinical and Translational Research (ICTR) for future studies.

Blood samples will be obtained from two sources:

  1. Leftover/discarded whole blood samples that were obtained for standard of care.
  2. Blood samples consisting of 1-5 tubes (3-20 ml of whole blood) from patients with written consent. When possible, these samples will be obtained during routine blood draws performed for a typical visit. It may be necessary to ask patients to specifically donate blood for the study.

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
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Above 12 years of age and referred to the Hematology Division at Montefiore-Einstein
  • Under the care of a Montefiore-Einstein hematologist for a hematologic disorder

排除标准

  • - Do not meet the Inclusion Criteria listed above

结局指标

主要结局

Biobank

时间窗: 5 years

To have specimens available for IRB approved studies

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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