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Robot-Assisted hernia surgery shows promise in small trial

NCT ID NCT07071740

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a robot called Dexter to help surgeons repair ventral hernias (bulges in the belly wall). Thirty-three adults with small to medium hernias took part. The main goals were to see if the robot was safe and could complete the surgery without switching to other methods.

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

33 people

The number who actually took part.

Started

Jun 2025

Finished

Jan 2026

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

Adult patients undergoing incisional or primary ventral hernia repair

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: * Aged \> 18 years * Planned to undergo incisional and primary midline ventral (M2-M4; epigastric, umbilical and infraumbilical) hernia repair smaller and equal to 8cm * Patient agrees to perform the 30-day follow-up assessment, as per standard of care Exclusion Criteria: * Any planned concomitant procedures * Active anticoagulant treatment * Recurring hernia with mesh during primary hernia repair * Need for transversal abdominal release * Patients under corticosteroids or other immunosuppressive treatment * Loss of domain type of hernia * Previous incision extending from xiphoid process to pubic bone (= Median laparotomy M1 to M5) * M2 hernia extending to M1 and/or M4 hernia extending to M5 * Ongoing intra-abdominal infection or septic state * Abdominal fistulae * History of major\* abdominal or pelvic surgery

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Allgemein öffentliches Krankenhaus Spittal/Drau

    Spittal an der Drau, 9800, Austria

  • Artemed Klinikum München Süd

    München, 81379, Germany

  • GH Saintes - Saint-Jean-d'Angély Site de Saintes

    Saintes, 17100, France

  • Hirslanden Klinik Zürich

    Zurich, Switzerland

  • Kantonsspital Winterthur

    Winterthur, 8401, Switzerland

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