The study is non-randomized, multicenter international safety, performance and clinical benefit outcome assessment of ANEUFIX to treat patients with isolated type II endoleak in the presence of a growing AAA-sac following an EVAR procedure more than 6 months ago.
The investigational device is called ANEUFIX, which is a product treating the endoleak by blockage of backflowing blood vessels, i.e. by filling the endoleak void and nidus of feeding artery and exit of existing draining arteries.
ANEUFIX is a polymer that cures rapidly (2-4 min at 37°C) after injection into the AAA-sac close to the nidus.
| Condition | Abdominal Aortic Aneurysm, Endoleak |
|---|---|
| Treatment | ANEUFIX |
| Clinical Study Identifier | NCT03918460 |
| Sponsor | TripleMed B.V. |
| Last Modified on | 10 October 2022 |
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