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About
This study is intended to show that the application of the Accero® (heal) stent is safe within the given indication.
Enrollment
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Volunteers
Inclusion criteria
Any patient treated with ACCERO® (heal) Stent according to IFU and has signed the informed consent
Exclusion criteria
- Patient is participating in another clinical trial
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Central trial contact
Acandis GmbH
Data sourced from clinicaltrials.gov
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