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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
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.
A prospective clinical sample collection and future natriuretic peptide testing will be conducted in an emergency department only population. Patients presenting to the Emergency Department (ED) with signs and symptoms of acute heart failure will be approached for enrollment. Clinical and laboratory data will be collected to establish product performance and clinical concordance to adjudicated clinical diagnosis. Approximately 1800 evaluable subjects at geographically dispersed sites in the US will be enrolled in the study. Sample collection and testing of clinical samples with the Access Natriuretic Peptide assay will be performed under two separate protocols
Age
21 - No limit years
Sex
ALL
Healthy Volunteers
No
Beckman Coulter Site AJ
Loma Linda, California, United States
Beckman Coulter Site AL
Sacramento, California, United States
Beckman Coulter Site AB
Gainesville, Florida, United States
Beckman Coulter Site AG
Indianapolis, Indiana, United States
Beckman Coulter Site AN
Kansas City, Kansas, United States
Beckman Coulter Site AA
Detroit, Michigan, United States
Beckman Coulter Site AH
St Louis, Missouri, United States
Beckman Coulter Site AI
Albuquerque, New Mexico, United States
Beckman Coulter Site AE
Stony Brook, New York, United States
Beckman Coulter Site AK
Cleveland, Ohio, United States
Start Date
November 20, 2019
Primary Completion Date
May 31, 2022
Completion Date
September 30, 2022
Last Updated
February 14, 2023
2,370
ACTUAL participants
Access Immunodiagnostic Products
DIAGNOSTIC_TEST
Lead Sponsor
Beckman Coulter, Inc.
NCT07191730
NCT07484009
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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