Clinical outpatient control after valve-sparing hartoperatio

Completed

• Conditions: VSARR / valve sparing aortic vessel operation; 10046973; 10007593

• Registration Number: NL-OMON40813
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

•All patients aged 18 years or older who received a valve sparing root reimplantation (Tirone David) at the Erasmus MC since 2000
•Signed informed consent by the patient and the investigator.

Exclusion Criteria

•Patients who are unable or uncapable to give informed consent

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Reoperation </p><br>

Secondary Outcome Measures

Name	Time	Method
<p> Survival outcome and Quality of life and Valve related complications. </p><br>