NCT00541632

Brief Summary

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Oct 2007

Shorter than P25 for all trials

Geographic Reach
1 country

9 active sites

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2007

Completed
5 days until next milestone

First Submitted

Initial submission to the registry

October 6, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 10, 2007

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2008

Completed
Last Updated

December 2, 2024

Status Verified

November 1, 2024

Enrollment Period

5 months

First QC Date

October 6, 2007

Last Update Submit

November 27, 2024

Conditions

Methicillin Resistance

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (9)

Denver Health Medical Center

Denver, Colorado, 80204, United States

Location

Atlanta Institute for Medical Research, Inc.

Atlanta, Georgia, 30030, United States

Location

Evanston Northwestern Healthcare

Evanston, Illinois, 60201, United States

Location

University of Iowa

Iowa City, Iowa, 52242, United States

Location

University of Maryland

Baltimore, Maryland, 21201-1595, United States

Location

Wayne State University

Detroit, Michigan, 48201, United States

Location

Washington University

St Louis, Missouri, 63110, United States

Location

Wake Forest University

Winston-Salem, North Carolina, 27157-1042, United States

Location

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Location

Study Officials

  • Werner E Bischoff

    Wake Forest University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 6, 2007

First Posted

October 10, 2007

Study Start

October 1, 2007

Primary Completion

March 1, 2008

Study Completion

March 1, 2008

Last Updated

December 2, 2024

Record last verified: 2024-11

Locations

US(9)