New stent grafts aim to improve aneurysm repair outcomes
NCT ID NCT07295145
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing three types of Bentley stent grafts used to repair complex abdominal aortic aneurysms. Researchers will follow 150 adults for 12 months to see how well the grafts work and if there are any side effects. The goal is to improve the safety and success of this minimally invasive procedure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2031
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients having complex abdominal aortic aneurysms
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients having complex abdominal aortic aneurysms suitable for an endovascular repair with a fenestrated and/or branched aortic endovascular graft in combination with one Bentley bridging stent graft per reno-visceral artery in accordance with the IFU of BeFlared, BeGraft or BeGraft Plus. Use of different products for different target vessels is allowed. Use of stents from other manufacturers for other reno-visceral arteries is allowed. * Patient is capable and willing to sign the informed consent and agrees to fulfil follow-up requirements * Patients ≥18 years of age at the time of consent Exclusion Criteria: * Patients with contraindications as listed in the IFUs * Previous stenting of the target vessel * Extension/relining of Bentley BSGs * Prior EVAR procedure
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a new stent keep complex aortic aneurysms safely sealed?
- Can a Stick-On AI patch replace wires for heart monitoring after surgery?
- Stent-Graft device under scrutiny for aortic aneurysm and dissection repair