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NCT06274918

Reducing ESKAPE Transmission in the Operating Room

Reducing Intraoperative ESKAPE (Enterococcus, S. Aureus, Klebsiella, Acinetobacter, Pseudomonas, and Enterobacter Spp.) Transmission Via Use of an Evidence-Based, Hand Hygiene Program Optimized by OR PathTrac
University of Iowa·ClinicalTrials.gov·device·Device trialRecruiting
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Surgical Procedure, Unspecified
Drug/Device/Intervention
Personalized Body-Worn Alcohol Dispenser
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
University of Iowa
Location
Iowa City, United States of America
Timeline & enrollment
Phase
N/A
Start date
Feb 01, 2023
End date
Dec 01, 2024
Enrollment
40 participants
Primary outcome

ESKAPE transmission events with and without the body worn device

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.

ICD-10 classifications
Surgical procedure, unspecifiedMedical procedure, unspecifiedOther surgical proceduresDuring unspecified surgical and medical careDuring unspecified surgical and medical care
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06274918
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06274918 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Iowa and is currently Recruiting. The study focuses on Surgical Procedure, Unspecified. Target enrollment is 40 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.