Robotic vs. open hernia surgery: which is better for recovery?
NCT ID NCT05906017
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compared two ways to fix a ventral hernia (a bulge in the belly wall): traditional open surgery and robotic-assisted surgery. Fifty-six adults with midline hernias were randomly assigned to one method. Researchers looked at how long patients stayed in the hospital, pain, cosmetic results, satisfaction, and stress from surgery. The goal was to see which approach leads to better short- and long-term outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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56 people
The number who actually took part.
- Started
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May 2023
- Finished
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Oct 2025
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age≥18 * ASA 1-3 * Clinical and radiologic diagnosis of midline ventral hernia * Eligible to surgery according to a preoperative anaesthetic assessment * Informed consent * Able to understand written and oral Danish language Exclusion Criteria: * Incarcerated ventral hernia requiring emergency surgery * Pregnancy * Patients with chronic pain due to arthritis, migraine or other illness requiring regular intake of analgesics (paracetamol, NSAID, opiates etc). * Current cancer diagnosis * History of psychiatric or addictive disorder that prevents the patient from participating in the trial * Co-existing inflammatory disease * Co-existing immunological disease that requires medication of any kind * BMI \>40 kg/m2
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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
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Sygehus Sønderjylland
Aabenraa, Southern Denmark, 6200, Denmark
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