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

A Blood Collection From Patients Presenting in the Emergency Department and Prescribed a Brain Natriuretic Peptide (BNP) Laboratory Test

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02614209

Acronym

BNP

Enrollment

400

Registered

2015-11-25

Start date

2015-05-31

Completion date

2016-08-31

Last updated

2016-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

ED, BNP

Brief summary

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

Detailed description

Plasma samples are collected from a minimum of 400 subjects. Specimens are used to confirm the currently accepted BNP cut off as and aid in the diagnosis and assessment of HF. Stored specimens for future use in BNP assay development.

Interventions

DEVICEIn Vitro diagnostic tests

Prospective blood collection

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

21 Years to No maximum

Healthy volunteers

Inclusion criteria

* Males and females \>21 years of age * Able to understand and willing to provide informed consent * Present in to ED * BNP test requested

Exclusion criteria

* Males and females\< 21 years * Unable to provide informed consent * Not presenting to ED * hemolyzed sample

Design outcomes

Primary

Measure	Time frame	Description
Measure BNP	6 months	400 subjects

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026