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Clinical Performance Evaluation of AQT90 FLEX BNP and NT-proBNP

R

Radiometer

Status

Completed

Conditions

Heart Failure

Study type

Observational

Funder types

Industry

Identifiers

NCT01808872
DC-043652

Details and patient eligibility

About

The AQT90 FLEX B-type Natriuretic Peptide (BNP) and N-terminal pro B-type natriuretic peptide (NT-proBNP) Tests are in vitro diagnostic assays intended as an aid in the diagnosis and assessment of the severity of heart failure in point-of-care and laboratory settings. The purpose of the study is to establish the clinical performance of the AQT90 FLEX BNP and NT-proBNP assays for both whole blood and plasma in the intended use population.

Enrollment

569 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject is 21 years of age or older
  • Subject is able to understand information given, and willing and able to voluntarily give their consent to participate in this study
  • Subject has diagnosis of heart failure

Exclusion criteria

  • Subject has Acute Coronary Syndrome (ACS)
  • Subject has been diagnosed and/or treated for malignancy within past 6 months
  • Subject has had cardiac surgery within the past 4 weeks
  • Subject claim of pregnancy
  • Subject's prior participation in this study

Trial design

569 participants in 1 patient group

Heart Failure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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