About this trial
A prospective, single-arm, multi-centre registry to evaluate the safety and performance of Myval THV series using Transcatheter Aortic Valve Implantation (TAVI) procedure in patients with symptomatic severe native aortic valve stenosis.
Eligibility criteria
Qualifiers
Patient over the age of 18 years with symptomatic aortic stenosis (severe AS), intended to perform TAVI procedure using Myval THV series as assessed by Heart Team.
Patient has provided written informed consent as approved by the Ethics Committee (EC)
Patient is willing to undergo all registry procedures and follow-up requirements
Disqualifiers
Patients with hyper sensitivity or allergy to aspirin, heparin, clopidogrel, ticlopidine, cobalt, nickel, chromium, molybdenum or any contrast media.
Ongoing infective endocarditis or any similar infection.
Pregnant or lactating females.
Liver failure (Child-Pugh Class B or C)
Trial design
Treatments tested in this trial
- Myval THV series
Treatment groups
Sponsors and collaborators
Portuguese Association of Interventional Cardiology
Lead sponsor
Meril Life Sciences Pvt. Ltd.
Collaborator