New rapid test could help fight superbugs in veterans
NCT ID NCT02060513
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study tested a new rapid diagnostic tool to quickly identify antibiotic-resistant bacteria in wounded warriors and veterans. Over 2,200 participants provided samples from blood, lungs, or skin. The goal was to see if the test could accurately detect resistant bacteria faster than standard lab methods, helping doctors choose the right antibiotic sooner.
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 rapid test could help doctors choose the right antibiotic faster, reducing ineffective treatments and slowing antibiotic resistance.
- What could go wrong
- This is a diagnostic study, not a treatment trial. The test's accuracy may not be high enough in real-world settings, and it does not directly improve patient outcomes.
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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2,298 people
The number who actually took part.
- Start date
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Aug 2013
- Finished
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Nov 2016
- 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
Inpatients with a suspected infection.
- 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: * Age ≥ 18 years old. * Microbiology culture (respiratory, blood or tissue/skin) ordered during regular clinical care. Exclusion Criteria: * Insufficient sample volume available after clinical test completed.
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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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Denver Health Medical Center
Denver, Colorado, 80204, United States
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Denver Veterans Affairs Eastern Colorado Health Care System
Denver, Colorado, 80220, United States
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Washington Hospital Center
Washington D.C., District of Columbia, United States
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Other studies related to the condition(s) this trial covers.
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