Bicuspid Aortic Valve (BAV) Registry

University of Michigan5,000 enrolled

Overview

The purpose of this registry is to gather information on patients with bicuspid aortic valve disease.

The purpose of this registry is to gather information on patients with bicuspid aortic valve disease. The data collected in the registry will be used to assess patterns of aortic dilation, responses to medical therapy based on serial imaging and to assess for potential genetic markers of this disease

Study Type

OBSERVATIONAL

Enrollment

5,000

Conditions

Bicuspid Aortic Valve

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Any patient over the age of 18 who is able/willing to give informed consent with the diagnosis of bicuspid aortic valve disease, a family history of this disease or an ascending aortic aneurysm that is idiopathic can be included in the registry. Exclusion Criteria: * Patients unable or unwilling to give informed consent.

Locations (1)

Univeristy of Michigan

Ann Arbor, Michigan, United States

RECRUITING

Outcomes

Primary Outcomes

Characterizing patients with bicuspid aortic valve disease

Identifying patients with bicuspid aortic valve disease, assessing the effect of medical intervention.

Time frame: 30 years

Central Contacts

Bo Yang, MD, PhD

CONTACT

boya@med.umich.edu

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.