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Completed No phase listed Observational

Access Natriuretic Peptide Assay(s) Pivotal - Emergency Department Subject Enrollment and Specimen Collection

ClinicalTrials.gov ID: NCT04169815

Public ClinicalTrials.gov record NCT04169815. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 7:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Pivotal Evaluation of the Access Natriuretic Peptdie Assay(s) as an Aid in the Diagnosis and Assessment of Severity of Acute Heart Failure - Emergency Department Subject Enrollment and Specimen Collection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the pivotal study is to collect blood specimens and clinical data from patients suspected of having Heart Failure (HF), which will be tested at a future date on Natriuretic Peptide assay(s) to validate diagnostic cutoffs and assess HF severity.

Study identification

NCT ID
NCT04169815
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Beckman Coulter, Inc.
Industry
Enrollment
2,370 participants

Conditions and interventions

Conditions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 19, 2019
Primary completion
May 30, 2022
Completion
Sep 29, 2022
Last update posted
Feb 13, 2023

2019 – 2022

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Beckman Coulter Site AJ Loma Linda California 92354
Beckman Coulter Site AL Sacramento California 95817
Beckman Coulter Site AB Gainesville Florida 32608
Beckman Coulter Site AG Indianapolis Indiana 46202
Beckman Coulter Site AN Kansas City Kansas 66160
Beckman Coulter Site AA Detroit Michigan 48202
Beckman Coulter Site AH St Louis Missouri 63110
Beckman Coulter Site AI Albuquerque New Mexico 87106
Beckman Coulter Site AE Stony Brook New York 11794
Beckman Coulter Site AK Cleveland Ohio 44109
Beckman Coulter Site AF Columbus Ohio 43210
Oregon Health and Science University Portland Oregon 97208-3003
Beckman Coulter Site AC Charleston South Carolina 29425
Beckman Coulter Site AD Nashville Tennessee 37235
Beckman Coulter Site AM Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04169815, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 13, 2023 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04169815 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →