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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 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. The trial reports 3 study locations across 1 state.

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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.

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

Sponsor

Mary K Hayden

1 total trials

What the Registry Record Tells You About NCT06282510

The ClinicalTrials.gov registry entry for NCT06282510 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mary K Hayden, which has 1 total studies on file at ClinicalTrials.gov.

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 3 study locations spanning 1 distinct geographic area - top geographies include 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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