ANEUFIX for Endoleak Type II Repair

Status Recruiting

Clinical Trial Summary

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.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03918460
Study type	Interventional
Source	TripleMed B.V.
Contact	Tjeerd Homsma
Phone	+31 (0)6 29078003
Email	t.homsma@triple-med.com
Status	Recruiting
Phase	N/A
Start date	May 13, 2020
Completion date	February 2026

View Details

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