Smart dosing of antibiotics may cut infection risk after colon surgery
NCT ID NCT05253339
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether giving the antibiotic cefoxitin using a target-controlled infusion pump works better than the standard method to prevent surgical site infections in patients having colon or rectal surgery. About 2,500 adults took part. The goal was to see if the new method lowers infection rates.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cefoxitin
- What this could lead to
- If successful, this could show that target-controlled infusion reduces surgical site infections better than the standard method.
- What could go wrong
- This is a completed single-center trial; results may not apply to other hospitals or surgeries. The benefit over standard dosing may be small or absent.
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
-
2,494 people
The number who actually took part.
- Started
-
Apr 2022
- Finished
-
Aug 2025
- 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
-
20 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 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: * over 20 years old * Patients who are scheduled to undergo colon or rectal surgery * Patients scheduled to receive cefoxitin as a prophylactic antibiotic Exclusion Criteria: * Known allergies, hypersensitivity, or intolerance to cefoxitin * Patients with a history of receiving cefoxitin within 3 days of the scheduled surgery time * Patients receiving therapeutic antibiotics * eGFR \< 30 ml/min/1.73m2
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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
-
Asan Medical Center
Seoul, Songpa-Gu,, 05505, South Korea
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