Observational Study to Collect Data of Patient Which Recieving a TAVI in TAVI Procedure
NCT ID: NCT07215143
Last Updated: 2025-10-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
300 participants
OBSERVATIONAL
2026-01-31
2033-06-30
Brief Summary
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The trial will include around 300 patients from several European centres who are scheduled to undergo or have already undergone a TAVI-in-TAVI procedure with the Myval valve. Participation includes follow-up observation for a period of up to five years. Data collection will take place exclusively within the framework of regular medical care. This includes information on pre-existing conditions, the procedure, complications and subsequent hospital stays. Imaging examinations such as echocardiography or CT scans can also be centrally evaluated if they are performed routinely.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age: 18 years or more
* Informed consent has been obtained.
Exclusion Criteria
* Limited life expectancy \<12 months
* Foreseeable problems in performing follow-up visits
18 Years
ALL
No
Sponsors
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IHF GmbH - Institut für Herzinfarktforschung
OTHER
Responsible Party
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Other Identifiers
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BO-002
Identifier Type: -
Identifier Source: org_study_id
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