Aortic Stenosis Clinical Trial
Official title:
ACURATE Neo™ Aortic Bioprosthesis for Implantation Using the ACURATE TA™ LP Transapical Delivery System in Patients With Severe Aortic Stenosis
Trial of ACURATE neo(TM) Aortic Bioprosthesis for Implantation using the ACURATE TA(TM) LP Transapical Delivery System in Patients with Severe Aortic Stenosis for evaluating the Safety and performance of the study device
This is a single arm, prospective, multicenter non randomised and open trial of the treatment
of patients with severe aortic stenosis where conventional aortic valve replacement (AVR) via
open heart surgery is considered to be high risk. All patients will be followed up to 5 years
after the intervention.
The primary objective is to evaluate the safety and performance of the study device in
patients presenting with severe aortic stenosis considered to be high risk for surgery
Secondary objective is to evaluate adverse events and study device performance.
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