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New CT scans track stent movement inside the body to improve aneurysm treatment

NCT ID NCT07475260

Knowledge-focused Sponsor: University of Twente Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study will use special CT scans that track both the heartbeat and breathing to see how a stent graft moves inside the abdominal aorta after aneurysm repair. Twenty-five patients with complex aneurysms will be scanned before surgery, at discharge, and at 6 and 12 months after. The goal is to understand how these movements might affect the stent's long-term success.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help doctors design better stent grafts and improve long-term outcomes for patients with complex aortic aneurysms.
What could go wrong
This is a small, early-stage observational study, not a treatment trial. It may not lead to any direct changes in patient care.

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

About 25 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Jan 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of 25 patients with an abdominal aortic aneurysms to be treated with F-EVAR, aged \>65. The study population are patients from either Medisch Spectrum Twente (MST), Rijnstate Ziekenhuis, Jeroen Bosch Ziekenhuis, Amsterdam UMC, UMC Utrecht and Zuyderland Medisch Centrum.

Ages

65 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Asymptomatic AAA, * Age \> 65 * Indication for AAA treatment according to standard practice * Anatomic suitability for the fenestrated Treo stent graft * At least one stentable main renal artery and one other stentable renal or mesenteric artery * Being able to hold their breath for 10 seconds. Exclusion Criteria: * No informed consent obtained * eGFR \< 30 ml/min * Allergy for intra venous contrast fluid.

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Conditions

The condition(s) this trial relates to.

abdominal aortic aneurysm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Abdominal aortic aneurysm Endovascular abdominal aortic aneurysm repair Fenestrated endovascular aortic repair

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    6 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • Amsterdam UMC

    Amsterdam, North Holland, 1105AZ, Netherlands

  • Jeroen Bosch Ziekenhuis

    's-Hertogenbosch, North Brabant, 5223 GZ, Netherlands

  • Medisch Spectrum Twente

    Enschede, Overijssel, 7512KZ, Netherlands

  • Rijnstate Ziekenhuis

    Arnhem, Gelderland, 6815AD, Netherlands

  • UMC Utrecht

    Utrecht, Utrecht, 3584 CX, Netherlands

  • Zuyderland Medisch Centrum

    Heerlen, 6419PC, Netherlands

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