Status:
COMPLETED
Evaluation of Two Hand Hygiene Products in ICUs
Lead Sponsor:
Solventum US LLC
Collaborating Sponsors:
3M
Conditions:
Hand Hygiene Effectiveness
Eligibility:
All Genders
18-70 years
Phase:
PHASE4
Brief Summary
This study will evaluate the immediate antimicrobial efficacy and persistence of two hand hygiene products on ICU Health Care Worker's skin flora by measuring bacterial organisms on hands using the ha...
Detailed Description
Crossover study with 50 Health care workers using each product with a minimum of 3 days in between. Products will be applied twice as per manufacturer's instructions for a Healthcare Personnel Handwas...
Eligibility Criteria
Inclusion
- HCW willing to participate in the study
- HCW willing to use non-Triclosan soap when soap is necessary throughout the study
- HCW who will don gloves prior to ICU patient room entry
Exclusion
- Use of any CHG -containing products ( liquid hand soap, Sage wipes) on the ICU 72 hours prior to study initiation and throughout study
- HCW with patient bandage or other dressing on palm(s)
- Known sensitivity or allergy to CHG or alcohols in hand hygiene products
- Known sensitivity or allergy to the following components: Lecithin, Polysorbate 80,Trypticase Soy Agar, sodium bisulfate, sodium thioglycollate, sodium thiosulfate
- History of skin allergies
Key Trial Info
Start Date :
October 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2015
Estimated Enrollment :
51 Patients enrolled
Trial Details
Trial ID
NCT02258412
Start Date
October 1 2014
End Date
February 1 2015
Last Update
October 23 2024
Active Locations (1)
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1
Cleveland Clinic
Cleveland, Ohio, United States, 44195