Suspended

BacLite Rapid MRSA Clinical Performance

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: October 2007
See protocol details

Summary

Principal SponsorSolventum US LLC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2007

Actual date on which the first participant was enrolled.

The purpose of this study is to compare the performance of the 3M(TM) BacLite (TM) Rapid MRSA test system to traditional culture methods in detecting the presence of Methicillin Resistant Staphylococcus aureus (MRSA) directly from nasal samples.

Official TitleBacLite Rapid MRSA Clinical Performance
Principal SponsorSolventum US LLC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: * Subjects 18 years or older * Subjects willing to document demographic characteristics * Subjects willing to have their nose swabbed * Subjects (or legal representative) willing to sign consent and authorization forms Exclusion Criteria: * Subjects who use Vicks Sinex Nasal spray or other nasal sprays * Subjects with prescribed nasal medical devices where collecting samples may resent more than minimal risk to subjects * Subjects having nasal prosthetics, jewelry or trauma to the nose or anything that may prevents sampling the anterior nares * Investigator believes that subject is unsuitable for inclusion.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 9 locations

Suspended

Denver Health Medical Center

Denver, United StatesOpen Denver Health Medical Center in Google Maps
Suspended

Atlanta Institute for Medical Research, Inc.

Atlanta, United States
Suspended

Evanston Northwestern Healthcare

Evanston, United States
Suspended

University of Iowa

Iowa City, United States
Suspended9 Study Centers