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Aneurysm repair Follow-Up: which scan is best?

NCT ID NCT07581392

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at 405 patients who had a minimally invasive procedure to fix an abdominal aortic aneurysm. Researchers reviewed medical records to see how often complications occurred and which imaging test—ultrasound or CT scan—was better at finding them. The goal was to improve follow-up care after aneurysm repair.

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

405 people

The number who actually took part.

Started

Jan 2026

Finished

Mar 2026

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

This study will utilize an existing dataset at UHL which contains surveillance \& follow-up information for patients who underwent EVAR procedures for AAA or iliac aneurysms between March 2006 and December 2024.

Ages

16 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: Included in registry of patients under surveillance with UHL Department of Vascular Surgery Under surveillance from March 2006 - December 2024 Underwent EVAR for AAA or iliac aneurysm repair Surveillance performed with both CDUS and CTA with reports available Exclusion Criteria: Not in registry for EVAR surveillance Not under surveillance during study period Underwent open repair for AAA or iliac aneurysm Both CDUS and CTA not available \-

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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.

Contacts and locations

Locations

  • University Hospital Limerick

    Limerick, Munster, V94 F558, Ireland

More trials for these conditions

Other studies related to the condition(s) this trial covers.