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Atrial Fibrillation, Stroke, and Bleeding in Patients Undergoing Aortic Biovalve Implantation (CAREAVR)

U

University of Turku

Status

Completed

Conditions

Atrial Fibrillation
Stroke
Transient Ischemic Attack
Aortic Stenosis
Bleeding

Study type

Observational

Funder types

Other

Identifiers

NCT02626871
T39/2015

Details and patient eligibility

About

The primary purpose of the FIN-bioAVR registry is to assess the incidence of AF, strokes and major bleeding events in patients undergoing aortic valve replacement. This retrospective multicenter registry will include 850 patients with aortic valve replacement using bioprosthesis.

Enrollment

850 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients undergoing aortic valve bioprosthesis implantation

Exclusion criteria

  • mechanical heart valves in any position

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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