Status:
COMPLETED
ProvodineTM Decreases Hand Contamination
Lead Sponsor:
Sundara Reddy
Collaborating Sponsors:
Microdermis Corporation
Conditions:
Hand Hygiene
Eligibility:
All Genders
22-65 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to see whether Provodine, an FDA approved product, provides long-lasting protection on the hands of staff who provide anesthesia for patients. If this product does provide...
Detailed Description
During the pre-intervention or baseline period, the investigators will do bag broth cultures of anesthesia providers' hands just before the start of their first case of the day (n =25). The participan...
Eligibility Criteria
Inclusion
- \- Must be an anesthesia provider at The University of Iowa Hospitals and Clinics
Exclusion
- \- Are not an anesthesia provider at The University of Iowa Hospitals and Clinics
Key Trial Info
Start Date :
December 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2014
Estimated Enrollment :
31 Patients enrolled
Trial Details
Trial ID
NCT04023682
Start Date
December 1 2013
End Date
November 1 2014
Last Update
August 2 2021
Active Locations (1)
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1
University of Iowa
Iowa City, Iowa, United States, 52242