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Study identifier: NCT03143361 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective European Multicenter Study on Aortic Valve Replacement: (E-AVR Registry)

Condition: Aortic Valve Stenosis · Valve Heart Stenosis  ·  Sponsor: University of Parma

PhaseN/A
Planned participants8000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Traditional and transcatheter surgical treatments of severe aortic valve stenosis (SAVS) are increasing in parallel with the improved life-expectancy. Recent randomized trials (RCTs) reported comparable or non-inferior mortality with transcatheter treatments compared to traditional surgery. However, RCTs have the limitation of being a mirror of the predefined inclusion/exclusion criteria, without reflecting the "real clinical world". Technological improvements have recently allowed the development of minimally invasive surgical accesses and the use of sutureless valves, but their impact on the clinical scenario is difficult to assess because of the monocentric design of published studies and limited sample-size. A prospective multicentre registry including all patients referred for a surgical treatment of SAVS (traditional, through full-sternotomy; minimally-invasive; or transcatheter; with both "sutured" and "sutureless" valves) will provide a "real-world" picture of available results of current surgical options, and will help to clarify the "grey zones" of current guidelines. E-AVR is a prospective observational open registry designed to collect all data from patients admitted for SAVS, with or without coronary artery disease, in 16 cardiac surgery Centres located in six countries (France, Germany, Italy, Spain, Switzerland, and United Kingdom). Patients will be enrolled over a 2-year period and followed-up for a minimum of 5 years to a maximum of 10 years after enrolment…

This description comes directly from the study's public registry record.

Talk to the study team

Francesco Onorati, MD, PhD  ·  (+39) 045 812 33 07  ·  francesco.onorati@univr.it

Always discuss trial participation with your own doctor first.

Locations (1)

University of VeronaVerona, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT03143361