Reducing bacterial 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
This study is testing if a personal alcohol dispenser can help reduce the spread of harmful bacteria in the operating room during surgeries to keep patients safer from infections.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Iowa Academic / other |
| Locations | 1 site (Iowa City, Iowa) |
| Trial ID | NCT06274918 on ClinicalTrials.gov |
What this trial studies
This study examines how a personalized, body-worn alcohol dispenser can impact the transmission of ESKAPE pathogens in the anesthesia work area during surgeries requiring general anesthesia. It builds on existing evidence regarding the epidemiology of perioperative bacterial transmission and healthcare-associated infections (HAIs). The study aims to implement a multi-faceted program to improve hand hygiene and reduce the risk of infections during surgical procedures. By analyzing the effectiveness of this intervention, the researchers hope to demonstrate a significant reduction in bacterial transmission and subsequent HAIs.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients undergoing surgeries that require general anesthesia and peripheral IV or central line placement.
Not a fit: Patients who are pediatric or do not require general anesthesia and/or IV/central line placement may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the incidence of healthcare-associated infections in surgical patients.
How similar studies have performed: Other studies have shown success in improving hand hygiene practices in healthcare settings, suggesting potential for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Iowa City, Iowa
- University of Iowa — Iowa City, Iowa, United States (Recruiting)
Study contacts
- Principal investigator: Andrew Pugely, MD — University of Iowa
- Study coordinator: Crystal J Maldonado, BA
- Email: crystal-maldonado@uiowa.edu
- Phone: 7736643889
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.