Condition: Severe Aortic Valve Stenosis · Sponsor: IRCCS Policlinico S. Donato
The general objective of this study is to compare in vitro and in vivo the hemodynamic performance of different types of aortic valve prostheses and possible surgical implantation techniques. The study involves the collection of data deriving from tests and procedures foreseen by normal clinical practice, including a transthoracic color Doppler echocardiogram, to which is added a 4DFlow cardiac MRI (magnetic resonance imaging) without contrast medium, to be performed between 1 and 3 months after the operation. The study will last 24 months and the patients involvement will end approximately 1-3 months after the intervention. There are no direct benefits expected from participation in the study. However, the instrumental data obtained by echocardiogram and Magnetic Resonance Imaging will be useful for monitoring the medium-term surgical outcome of patients after surgery.
This description comes directly from the study's public registry record.
Agnese Rossi, Study Coordinator · 00393409009040 · agnese.rossi@grupposandonato.it
Giacomo Bortolussi, Researcher - Cardiac Surgeon · 003900393246943755 · giacomo.bortolussi@grupposandonato.it
Always discuss trial participation with your own doctor first.
| Policlinico di Bari | Bari, Apulia, Italy | Recruiting |
| IRCCS Policlinico San Donato | San Donato, Lombardy, Italy | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06859255