RecruitingPhase 4NCT06282510

Nasal Antisepsis for C. Auris Prevention

Impact of Nasal Antisepsis on Candida Auris Colonization


Sponsor

Mary K Hayden

Enrollment

120 participants

Start Date

Jan 29, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether applying 10% povidone iodine (a common antiseptic) inside the nose twice daily for up to 5 days can reduce nasal colonization and skin spread of Candida auris, a highly drug-resistant fungus that can cause serious infections in hospitalized patients. C. auris spreads easily in healthcare settings, and decolonization strategies are urgently needed to prevent outbreaks. Eligible participants are hospitalized adults (in long-term acute care or acute care hospitals in the Chicago area) who are already known to carry C. auris in their nose, speak English, and are not allergic to iodine or currently pregnant. Participation involves swabs to confirm C. auris colonization, then random assignment to receive either the nasal iodine treatment or no intranasal treatment, with follow-up swabs taken over the course of the hospital stay. This summary was prepared using AI to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPovidone Iodine Topical

Topical intranasal povidone iodine (10%) twice daily for 5 days


Locations(3)

Rush University Medical Center

Chicago, Illinois, United States

RML Specialty Hospital

Chicago, Illinois, United States

RML Specialty Hospital

Hinsdale, Illinois, United States

View Full Details on ClinicalTrials.gov

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NCT06282510


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