RECRUITING

Reducing Intraoperative ESKAPE Transmission Through Use of a Personal Hand Hygiene System

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The investigators hypothesize that the use of a personal hand hygiene system (SafeHavenTM) by anesthesia providers in the adult operating room, combined with a novel infectious pathogen tracking system (OR PathTrac) will decrease participant exposure to pathologic bacteria in the adult operating room.

Official Title

Reducing Intraoperative ESKAPE (Enterococcus, S. Aureus, Klebsiella, Acinetobacter, Pseudomonas, and Enterobacter Spp.) Transmission in the Adult Operating Room Via Use of a Personal Hand Hygiene System Optimized by OR PathTrac

Quick Facts

Study Start:2022-01-01
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04900298

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Patients with a known infection at the time of surgery.
  2. * Prisoners
  3. * Pregnant Women
  4. * Patients lacking capacity to consent
  5. * Patients with an allergy to a component of hand hygiene solution, such as ethyl alcohol
  6. * Refusal of consent

Contacts and Locations

Study Contact

Brandon M Togioka, MD
CONTACT
503-494-4572
togioka@ohsu.edu
Sydney Rose, MD
CONTACT
503-494-1358
rosesy@ohsu.edu

Principal Investigator

Brandon M Togioka, MD
PRINCIPAL_INVESTIGATOR
Oregon Health and Science University

Study Locations (Sites)

Oregon Health and Science University
Portland, Oregon, 97239
United States

Collaborators and Investigators

Sponsor: Oregon Health and Science University

  • Brandon M Togioka, MD, PRINCIPAL_INVESTIGATOR, Oregon Health and Science University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-01-01
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2022-01-01
Study Completion Date2026-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Surgical Wound Infection
  • Cross Infection