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Can a single robotic incision fix hernias with less pain and better looks?

NCT ID NCT07755657

Disease control Sponsor: Algemeen Ziekenhuis Maria Middelares Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 10, 2026 · Last updated Aug 21, 2026 · Updated 2 times

Summary

This trial is testing a new robotic method for repairing ventral hernias (bulges in the belly wall) using a single small incision above the pubic bone. The approach, called SP2 eTEP, uses the da Vinci Single Port system to place a mesh to strengthen the abdominal wall. Researchers will measure how long the surgery takes, any technical problems, and complication rates, as well as patients' quality of life and body image after the procedure. The study includes adults with certain types of midline hernias, with or without a separation of the abdominal muscles.

What this could mean

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

Active substance
Robotic suprapubic extraperitoneal single-port (SP2 eTEP) ventral hernia repair using the da Vinci Single Port surgical system
What this could lead to
If successful, this approach could offer a less invasive, potentially faster-recovering option for ventral hernia repair, with improved cosmetic outcomes.
What could go wrong
This is a small, early-stage study. The procedure is technically demanding and may carry risks such as complications, device issues, or longer surgery times. Results may not apply to all hernia types.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

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

Started

Mar 2026

Expected to finish

Dec 2027

An estimate. End dates often move.

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.

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: * Adults with a primary midline ventral (umbilical or epigastric) classified as M1-M4 according to EHS classification with or without concomitant diastasis of the rectus abdominis muscles Exclusion Criteria: * Post-prostatectomy * Post-preperitoneal mesh operation for inguinal hernia * Laparotomy in the lower abdomen * Caesarean section * Pregnancy * Contra-indication for general anaesthesia

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As listed by the trial registrant

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

Ventral hernia repair

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • AZ Maria Middelares

    RECRUITING

    Ghent, East-Flanders, 9000, Belgium

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