An International Registry for Data and Imaging of Children with Congenital Bicuspid Aortic Valve Disease


About this study

The purpose of this registry is to collect data and imagery, to study children and adults under the age of 21 who were born with bicuspid aortic valve disease. Some types of bicuspid aortic valves might be more likely associated with greater disease severity such as the degree of stenosis or valve leakage and possible enlargement of the aorta.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

  • Age 0-21 years
  • Identified as having a bicuspid aortic valve by echocardiographic, CT or MRI
    • Criteria will be included in the data repository for the BAVCon limited dataset
    • BAVCon will modify their protocol for a pediatric core

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Donald Hagler, M.D.

Closed for enrollment

More information


Publications are currently not available

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