Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT06282510

Nasal Antisepsis for C. Auris Prevention

Led by Mary K Hayden · Updated on 2025-10-15

120

Participants Needed

3

Research Sites

252 weeks

Total Duration

On this page

Sponsors

M

Mary K Hayden

Lead Sponsor

R

Rush University Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a randomized, controlled, open-label trial of effect of 10% povidone iodine intranasal antisepsis on the detection of Candida auris.

CONDITIONS

Official Title

Nasal Antisepsis for C. Auris Prevention

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • History of C. auris colonization or infection
  • Patient in a participating facility
Not Eligible

You will not qualify if you...

  • History of severe allergy to iodine-based products, defined as anaphylaxis or rash
  • Currently breastfeeding or pregnant
  • Non-English language speaking

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Rush University Medical Center

Chicago, Illinois, United States, 60612

Actively Recruiting

2

RML Specialty Hospital

Chicago, Illinois, United States, 60624

Actively Recruiting

3

RML Specialty Hospital

Hinsdale, Illinois, United States, 60521

Actively Recruiting

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Research Team

S

Sarah E. Sansom, DO

CONTACT

M

Mary K. Hayden, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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