Nasal Antisepsis for C. Auris Prevention
Recruiting now · Phase 4
Conditions studied: Candida Auris Infection, Colonization, Asymptomatic
In brief
This is a randomized, controlled, open-label trial of effect of 10% povidone iodine intranasal antisepsis on the detection of Candida auris.
Key facts
- Study ID
- NCT06282510
- Run by
- Mary K Hayden
- People needed
- 120
- Starts
- 2024-01-29
- Expected to finish
- 2028-12-01
- Last updated by the study team
- 2025-10-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- History of C. auris colonization or infection
- Patient in a participating facility
You may not qualify if…
- History of severe allergy to iodine-based products, defined as anaphylaxis or rash
- Currently breastfeeding or pregnant
- Non-English language speaking
Where it is running
- Rush University Medical Center — Chicago, Illinois, United States (enrolling)
- RML Specialty Hospital — Chicago, Illinois, United States (enrolling)
- RML Specialty Hospital — Hinsdale, Illinois, United States (enrolling)
Full record on ClinicalTrials.gov
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