Complex Abdominal Aortic Aneurysm Clinical Trial
Official title:
Compassionate Use Treatment for a Single Patient With a Custom Made Branched/Fenestrated Endovascular Device for the Treatment of Complex Abdominal Aortic Aneurysm
The FENESTRATED AAA ENDOVASCULAR GRAFT WITH THE H&L-B ONE-SHOTâ„¢ INTRODUCTION SYSTEM is neither commercially available or available as part of a clinical trial. IRB approval of this protocol was requested so that Cook, Incorporated may apply to the FDA for approval for one-time use of this patient-specific device for compassionate use for patient AO. It is a custom made endovascular device consisting of4 fenestrations for the celiac, SMA (superior mesenteric) and left and right renal arteries.
The Custom Made Branched/Fenestrated Endovascular Device to be used in this treatment plan
is not Food and Drug Administration (FDA)-approved, and is approved for use only in a
clinical study. However, the FDA has allowed the use of this device for compassionate use.
The devices used are tubular grafts made of polyester fabric sewn to metal stents. The upper
part of the grafts includes fenestrations (holes) that allow the grafts to be located above
or near major arteries that branch off of the aorta (celiac artery, superior mesenteric
artery (SMA), and renal arteries) without blocking blood flow to them. The celiac artery
supplies blood to internal organs including the liver and stomach. The SMA supplies blood to
internal organs as well, including parts of the large and small intestines. The renal
arteries supply blood to the kidneys. Grafts with branches and/or fenestrations are needed
when the aneurysm is located near these major arteries. The major arteries that branch off
of the aorta (celiac artery, SMA, and renal arteries) may also be treated using stents
(small tubular metal structures) to help keep the arteries open and aligned with the graft
fenestrations (holes).
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Status | Clinical Trial | Phase | |
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Recruiting |
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