The Global cVAD Registry


About this study

The goal of the global cVAD registry is to collect clinical, procedural and outcome data from hospital medical records for patients who received one or multiple Impella devices in routine clinical care, across all participating sites without preselection.

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.

The population to be enrolled in this registry includes patients who received mechanical circulatory support with the Impella devices per the institution’s standard of care and treating physician’s discretion.

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

Patricia Best, M.D.

Closed for enrollment

More information


Publications are currently not available

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