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Glue instead of stitches? new study tests mesh fixation for hernia repair

NCT ID NCT07295379

Knowledge-focused Sponsor: Advanced Medical Solutions Ltd. 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 09, 2026 · Updated 2 times

Summary

This study looks at a medical glue called LiquiBand FIX8 that is already approved in Europe. It is used to hold mesh in place during surgery for ventral incisional hernias, which can happen after a previous surgery. The goal is to see how safe and effective the glue is by checking if the hernia comes back within 12 months. About 148 adults who had this type of hernia repair will have their medical records reviewed.

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 148 people

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

Started

Feb 2026

Expected to finish

Jul 2026

An estimate. End dates often move.

Lead sponsor

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

All comers for ventral incisional hernia repair at Royal Lancaster Infirmary performed by study Investigator

Ages

18 to 80 years

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: * Patient is ≥ 18 years of age and ≤ 80 years of age. * Patient had a ventral incisional hernia (this may include both primary and recurrent). * Patient underwent a ventral incisional repair and LIQUIBAND FIX8® adhesive was used for mesh fixation (including those patients where supplemental fixation was used) * Has a minimum of 12 months follow-up. Exclusion Criteria: * Concomitant parastomal hernia repair * No other exclusions specific to the device

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As listed by the trial registrant

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

Hernia incisional ventral

Contacts and locations

Locations

  • Royal Lancaster Infirmary

    Lancaster, LA1 4RP, United Kingdom

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