Detection of Chlamydia (CT) and Gonorrhea (NG)

NCT02055742 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 700

Last updated 2017-12-07

No results posted yet for this study

Summary

To evaluate the illumigene Chlamydia and illumigene Gonorrhea assays, using the illumipro-10, with male urine, female urine, physician-collected (medical professional) endocervical swabs and self-collected vaginal swabs taken from symptomatic and asymptomatic patient populations.

Conditions

  • Chlamydia
  • Gonorrhea

Interventions

DEVICE

illumigene CT and NG assays, illumipro-10

Sponsors & Collaborators

  • Meridian Bioscience, Inc.

    lead INDUSTRY

Eligibility

Min Age
14 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-03-01
Primary Completion
2014-09-09
Completion
2014-09-09

Countries

  • United States

Study Locations

More Related Trials

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 NCT02055742 on ClinicalTrials.gov