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New No-Stitch mesh could change hernia surgery

NCT ID NCT06915155

Disease control Sponsor: Swissmed Hospital 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 21, 2026 · Updated 1 time

Summary

This study is testing a new mesh called Swing-Mesh™ for fixing groin hernias. The mesh is designed to stay in place without stitches or glue. About 300 adults having planned hernia surgery will get this mesh. Researchers will check for hernia return, pain, and other problems over 6 months.

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

323 people

The number who actually took part.

Started

Apr 2025

Finished

Aug 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

Patients scheduled for elective laparoscopic-endoscopic inguinal hernia repair using the Swing-Mesh™ implant. The study population includes adult patients of both sexes who meet the inclusion criteria and do not have any of the specified exclusion criteria. Participants will be recruited from surgical centers in Poland.

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: * elective groin hernia repair * age \> 18 years * male and female patients can participate * eligibility for laparoendoscopic repair * signed written informed consent Exclusion Criteria: * age \<18 years * emergency surgery (incarcerated hernia) * contaminated surgical field * recurrent hernia * extremely large scrotal hernias with the need of other abdominal compartment syndrome (ACS) preventive procedures (botulin injection, bowel resection, preoperative progressive pneumoperitoneum - PPP) * M3 or M3+L1-3 (EHS classification) groin hernia confirmed during surgery

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Conditions

The condition(s) this trial relates to.

Hernia Hernia, Inguinal

As listed by the trial registrant

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

Inguinal hernia

Contacts and locations

Locations

  • Swissmed Hospital

    Gdansk, Gdańsk, 80-215, Poland

  • Swissmed Hospital

    Gdansk, 80-280, Poland

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