跳至主要内容
临床试验/NCT01026571
NCT01026571进行中(未招募)不适用

Identification of Genetic Causes of Bicuspid Aortic Valve Disease

Boston University1 个研究点 分布在 1 个国家目标入组 4,000 人开始时间: 2009年12月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
4,000
试验地点
1
主要终点
Identification of genetic variants associated with the occurrence of bicuspid aortic valve disease

研究概览

简要总结

BAVgenetics is a partnership between Investigators at Boston University, Brigham and Women's Hospital, and Massachusetts General Hospital dedicated to discovering the genetic causes of bicuspid aortic valve disease and associated aortic disease.

详细描述

The Investigators at BAVgenetics are dedicated to discovering the mechanisms of bicuspid aortic valve disease and why individual genetics seem to play such an important role in generation of this disease.

If you have, or have had, a bicuspid aortic valve, we seek your help in this effort by volunteering to donate DNA to the BAV Registry, so that this disease can be better understood and therapies for it can be developed.

The BAV Registry is comprised of patients who have donated DNA collected from saliva (spit) and have provided us with personal health information that tells us about their bicuspid aortic valve.

Individuals in the Registry have signed the consent form, filled out the medical history questionnaire and the authorization form, and provided DNA via our saliva sample kits.

We will send you the requisite forms so that you receive the most up-to-date information about the study as older forms may be outdated. We also need paper copies of the forms; therefore, we send all the forms via ground mail along with a pre-paid return envelope for your convenience.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
14 Years 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any adult patient ≥ 14 years of age may be recruited regardless of gender, ethnicity or racial group.
  • Patients with a diagnosis of bicuspid aortic valve will be enrolled.
  • Patients who have had their bicuspid aortic valve previously replaced will also be enrolled.
  • Relatives of patients with a diagnosis of bicuspid aortic valve are also welcomed to be enrolled regardless if they have BAV or not, as it is helpful to examine the DNA of first degree relatives.

排除标准

  • Non-English speaking

结局指标

主要结局

Identification of genetic variants associated with the occurrence of bicuspid aortic valve disease

时间窗: 20 years

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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