Evaluation of the Performance of the Cobas CT/NG Test for Use on the Cobas 6800/8800 Systems for Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Male and Female Urogenital Samples

Author:

Van Der Pol Barbara1ORCID,Fife Kenneth2,Taylor Stephanie N.3,Nye Melinda B.4,Chavoustie Steven E.5,Eisenberg David L.6,Crane LaShonda7,Hirsch Gregory8,Arcenas Rodney9,Marlowe Elizabeth M.9

Affiliation:

1. University of Alabama at Birmingham, Birmingham, Alabama, USA

2. Indiana University School of Medicine, Indianapolis, Indiana, USA

3. Louisiana State University, New Orleans, Louisiana, USA

4. Laboratory Corporation of America Holdings, Burlington, North Carolina, USA

5. Healthcare Clinical Data, Inc., North Miami, Florida, USA

6. Planned Parenthood of St. Louis Region and Southwest Missouri, St. Louis, Missouri, USA

7. Planned Parenthood Gulf Coast, Inc., Houston, Texas, USA

8. Planned Parenthood of Northern, Central and Southern New Jersey, Inc., Morristown, New Jersey, USA

9. Roche Molecular Systems, Inc., Pleasanton, California, USA

Abstract

The clinical performance of the Cobas CT/NG assay on the Cobas 6800/8800 systems (Cobas) for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae was established in a multisite, prospective collection study using male and female urogenital specimens; supportive data from archived specimens were also included. The results obtained with the Cobas assay were compared with the patient infected status derived from a combination of U.S.

Funder

Roche Molecular Systems, Inc.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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