Blood Collection of Patient Presenting in the ED and Prescribed a BNP

NCT02614209 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2016-08-10

No results posted yet for this study

Summary

Plasma specimen collected from patients presenting in the Emergency Department (ED) with or without Heart Failure (HF) and prescribed a BNP.

Conditions

Interventions

DEVICE

In Vitro diagnostic tests

Prospective blood collection

Sponsors & Collaborators

  • Fujirebio Diagnostics, Inc.

    lead INDUSTRY

Principal Investigators

  • Diana Dickson, RAC · Fujirebio Diagnostics, Inc.

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-08-31
Completion
2016-08-31

Countries

  • United States

Study Locations

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Entities

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 NCT02614209 on ClinicalTrials.gov