CompletedNot Applicable

Reducing ESKAPE Transmission in the Operating Room

United States39 participantsStarted 2023-02-01

Plain-language summary

This study is designed to examine the impact of a personalized, body worn alcohol dispenser on the epidemiology of ESKAPE transmission in the anesthesia work area for patients undergoing surgery requiring general anesthesia.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Adult patients undergoing surgery requiring general anesthesia and peripheral IV and/or central line placement. Exclusion Criteria: Pediatric patient, not requiring general anesthesia and/or IV/central line placement.

What they're measuring

ESKAPE transmission events with and without the body worn device

Timeframe: Up to 96 hours from the surgial procedure

Trial details

NCT IDNCT06274918

SponsorUniversity of Iowa

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-09-13

View on ClinicalTrials.gov More Surgical Procedure, Unspecified trials