Multi-center Evaluation of the VERSANT® CT/GC DNA 1.0 Assay (kPCR)in Detecting C. Trachomatis and N. Gonorrhoeae

NCT01167777 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 2296

Last updated 2015-11-26

No results posted yet for this study

Summary

Multicenter clinical study to test a new qualitative in vitro nucleic acid amplification assay based on kPCR technology. The assay is intended for the diagnosis of Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (GC).

Conditions

  • Chlamydia
  • Gonorrhea

Sponsors & Collaborators

  • Siemens Healthcare Diagnostics Inc

    lead INDUSTRY

Principal Investigators

  • NORMAND DESPRES, PhD · Siemens Healthcare Diagnostics

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2010-12-31
Completion
2010-12-31

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 NCT01167777 on ClinicalTrials.gov