AQT90 FLEX NTproBNP2 Test Kit Method Comparison Study

Radiometer

Status: Enrolling

Conditions: Diagnostic Test

Study type: Observational

Funder types: Industry

Identifiers

NCT06693050

DC-087457

Details and patient eligibility

About

The purpose of this study is to verify performance claims for method comparison for the NTproBNP2 Test Kit on the AQT90 FLEX analyzer in whole blood (WB) and plasma (PL).

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects must be able to understand given information and demonstrate willingness and ability to voluntarily give a signed, valid written informed consent to participate in the study.
• Subjects must be 18 years of age or older.
• Subjects with expected NT-proBNP concentrations within the measuring range of NTproBNP2 assay.

Exclusion criteria

• Subjects known to be pregnant or breast-feeding.
• Subjects previously enrolled in the study.
• Subject, who has withdrawn consent.