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NCT06282510 · ClinicalTrials.gov registry record · Phase 4

Nasal Antisepsis for C. Auris Prevention

A Phase 4 study of Candida Auris Infection and Colonization, Asymptomatic, sponsored by Mary K Hayden.

Recruiting
Registry status
Phase 4
Development phase
120
Enrollment target
3
Study locations

NCT06282510: Recruiting Phase 4 study of Candida Auris Infection and Colonization, Asymptomatic, sponsored by Mary K Hayden.

NCT06282510 is a Phase 4 study of Candida Auris Infection and Colonization, Asymptomatic that is actively recruiting participants, run by Mary K Hayden. The registered enrollment target is 120 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06282510, a Phase 4 study of Candida Auris Infection and Colonization, Asymptomatic, is actively recruiting participants, sponsored by Mary K Hayden.

RECRUITING
Registry status
Phase 4
Development phase
120 participants
Enrollment target
3
Study locations

Study Summary

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

Primary Outcome

Culture detection of C. auris from anterior nares on intervention day 5.

Interventions

  • DRUG Povidone Iodine Topical

Study Locations (3)

Illinois

  • Rush University Medical Center - Chicago
  • RML Specialty Hospital - Chicago
  • RML Specialty Hospital - Hinsdale

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2024-01-29
Est. Completion 2028-12
Phase Phase 4
Mary K Hayden

1 total trials

What NCT06282510 shows while recruiting

NCT06282510 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower).

The record links to 2 conditions, with Candida Auris Infection appearing as the primary indexed condition, and to 1 intervention - of which Povidone Iodine Topical is the first listed.

NCT06282510 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06282510 about?

NCT06282510 is a clinical study titled "Nasal Antisepsis for C. Auris Prevention". This is a randomized, controlled, open-label trial of effect of 10% povidone iodine intranasal antisepsis on the detection of Candida auris.

What is the current status of trial NCT06282510?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2024-01-29. Estimated completion is 2028-12.

What conditions does trial NCT06282510 study?

This clinical trial studies the following conditions: Candida Auris Infection, Colonization, Asymptomatic.

What interventions are being tested in trial NCT06282510?

The interventions under investigation include: Povidone Iodine Topical (DRUG).

Who is sponsoring clinical trial NCT06282510?

This trial is sponsored by Mary K Hayden, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06282510 being conducted?

This trial has 3 study locations across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT06282510's enrollment target sits among peer trials

120 673rd of 2000 higher than 1,290 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06282510, the US trial registry maintained by the National Library of Medicine. NCT06282510 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.