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A Clinical Simulation Study of a Test Material on the Anterior Nares

NCT05617729 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2022-11-15

No results posted yet for this study

Summary

The objective of this study is simulate the clinical use of a test material within a 24h window. Efficacy will be simulated as the capacity of the material to reduce or clear the anterior nares bacterial population from opportunistic pathogens (e.g. Staphylococcus Aureus, Escherichia Coli, etc).

Conditions

  • Colonization, Asymptomatic

Interventions

OTHER

Saline applied via swab

sterile saline applied via swab

OTHER

Povidone-iodine based gel

gel applied via swab

Sponsors & Collaborators

  • Center for Innovation and Research Organization

    lead NETWORK

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-07
Primary Completion
2022-03-18
Completion
2022-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05617729 on ClinicalTrials.gov