QuickVue Influenza A + B Test Field Study

NCT03417869 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1381

Last updated 2018-03-20

No results posted yet for this study

Summary

Demonstrate improved clinical performance of visually read QuickVue Influenza A+B test.

Conditions

  • Influenza A, Influenza B

Interventions

DEVICE

QuickVue Influenza A+B

Rapid diagnostic test with IVD, QuickVue Influenza A+B

Sponsors & Collaborators

  • Quidel Corporation

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-16
Primary Completion
2018-02-01
Completion
2018-02-01
FDA Device
Yes

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 NCT03417869 on ClinicalTrials.gov