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Mesh fails to prevent hernias in aortic repair patients

NCT ID NCT07416422

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at whether placing a mesh during abdominal aortic aneurysm repair could prevent incisional hernias later. Fifty patients were split into two groups: one got mesh reinforcement, the other standard closure. After follow-up, the mesh did not show a clear benefit in preventing hernias.

What this could mean

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

Active substance
prophylactic onlay mesh
What this could lead to
If successful, this approach could reduce incisional hernias after open abdominal aortic aneurysm repair.
What could go wrong
The study was small (50 patients) and completed without showing a clear benefit. Results may not apply to all patients or surgical techniques.

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

50 people

The number who actually took part.

Started

Jan 2019

Finished

May 2023

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

Patients with AAA open repair between January 2019 and December 2021 in our institution.

Ages

18 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: * Patients who had open aortic surgery for AAA during the study period and gave their informed consent to participate in the study. Exclusion Criteria: * Urgent AAA repair * Patients treated for infective aortic aneurysms. * Different access to midline laparotomy.

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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

  • Hospital Ramón y Cajal

    Madrid, 28034, Spain

More trials for these conditions

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