Can audit and feedback curb unnecessary antibiotics in heart device surgeries?
NCT ID NCT05020418
First seen Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time
Summary
This study tests a program to help doctors avoid giving unnecessary antibiotics to patients undergoing heart device procedures, such as pacemaker or defibrillator implants. The program includes education, feedback on current practices, and comparisons with other hospitals. Researchers will measure whether the program reduces antibiotic misuse and related complications like infections and kidney injury.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a multi-faceted implementation bundle including audit and feedback, education materials, and facilitation
- What this could lead to
- If successful, this approach could reduce unnecessary antibiotic use and lower rates of infections and kidney injury in heart device patients.
- What could go wrong
- The intervention may not change prescribing habits, or the benefits seen at a few sites may not apply across the entire VA system.
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
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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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5,469 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Dec 2025
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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: * This study is open to any adult VA patient with data about a cardiac device procedure performed in the electrophysiology laboratory entered into the national VA EHR. Exclusion Criteria: * None
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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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VA Boston Healthcare System
Boston, Massachusetts, 02130, United States