Belly bug mystery: 300 patients help unlock why wounds get infected after surgery
NCT ID NCT06300892
First seen Jun 27, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study watches 300 adults having open abdominal surgery to understand why some get surgical site infections. Researchers will collect samples from the skin and gut during surgery and track patients for 30 days. By comparing those who get infections to those who don't, they hope to identify which bacteria cause the problem and where they come from.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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71 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Jun 2026
- 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.
Who is studied
adults over the age of 18 years, who are undergoing open abdominal surgery with a midline incision.
- 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.
Show the full entry requirements Hide 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: * We will include adult patients (age ≥ 18 years) * Undergoing open abdominal surgery during the study period. * Open abdominal surgery will include any abdominal procedure entering the peritoneal cavity through a midline incision with a skin incision that is 5cm or greater. Exclusion Criteria: * Patients with planned minimally invasive surgery including laparoscopic or robotic surgery as these patients have lower rates of surgical site infections (SSIs). Patients who have a laparoscopic or robotic surgery converted to open surgery will be excluded. * Appendectomy and cholecystectomy as these patients have lower risk of SSI. * Vascular, gynecological, obstetric, urological or transplantation. * Trauma patients. * Patients without source control at the index operation including those with an open abdomen, no fascial closure, or temporary abdominal closure device (such as abthera dressing). * Pediatric patients (age\<18 years). * Patients who decline swab/specimen collection.
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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
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University of Minnesota
Minneapolis, Minnesota, 55414, United States