Hospitals launch early warning system against superbugs
NCT ID NCT05734391
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tracks infections that people get while in the hospital and monitors how germs become resistant to antibiotics. Researchers will collect swabs from 1,500 patients to test for resistant bacteria and build a national network to spot outbreaks early. The goal is to strengthen infection control and protect patients from hard-to-treat infections.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could create an early warning system to detect and contain dangerous antibiotic-resistant germs before they spread widely in hospitals.
- What could go wrong
- This is an observational surveillance study, not a treatment trial. It may not directly change patient care, and building a national network takes time and cooperation.
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
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About 1,500 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2022
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- 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
individuals being admitted to participating wards, of all clinical conditions, genders, and ages, meeting the inclusion/exclusion criteria
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * hospital inpatient admission to participating wards. Exclusion Criteria: * diagnosis of a bleeding disorder * platelet counts of \<50,000 * diagnosis of coagulopathy * presence of active bleeding * inability to have a nares swab collected due to some other condition where nasal swabbing would be contraindicated * inability to have a rectal swab collected due to some other condition where rectal swabbing would be contraindicated
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites in 2 countries. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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
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Princess Marina Hospital
Gaborone, 267, Botswana
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University of Pennsylvania School of Medicine
Philadelphia, Pennsylvania, 19104, United States
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