MedTrace Logo

Pilot Evaluation of the FilmArray® Febrile Infant (FI) Panel

NCT02477683 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1514

Last updated 2016-12-21

No results posted yet for this study

Summary

The purpose of this study is to collect data to support decisions made by BioFire regarding assay development, panel composition, and intended use for the final FilmArray FI reagent pouch. The study will utilize whole blood and/or plasma obtained from pediatric patients under 3 years of age that present with acute fever.

Conditions

  • Acute Fever

Sponsors & Collaborators

  • BioFire Diagnostics, LLC

    lead INDUSTRY

Eligibility

Max Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-31
Primary Completion
2016-10-31
Completion
2016-10-31

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 NCT02477683 on ClinicalTrials.gov