- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06905392
AQT90 FLEX NTproBNP2 Test Kit Matrix Comparison and Sample Stability Verification Study
February 16, 2026 updated by: Radiometer Medical ApS
The purpose of this study is to establish the correlation between sample matrices, and to determine the sample stability for the NTproBNP2 Test Kit on the AQT90 FLEX analyzer.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
154
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Murcia, Spain
- Hospital Universitario Virgen de La Arrixaca
-
Pamplona, Spain, 31008
- Clinica Universidad de Navarra
-
Santiago de Compostela, Spain
- Hospital Clinico Universitario de Santiago Compostela
-
Ùbeda, Spain
- Servicio Andaluz de Salud (SAS) - Hospital San Juan de la Cruz
-
-
-
-
Minnesota
-
Minneapolis, Minnesota, United States, 55404
- Hennepin Healthcare (Research Institute/ Minneapolis Medical Research Foundation)
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Patient population with expected NT-proBNP concentrations within the measuring range of NTproBNP2 Test Kit.
Description
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 Test Kit.
Exclusion Criteria:
- Subjects known to be pregnant or breast-feeding.
- Subjects previously enrolled in the study.
- Subject, who has withdrawn consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation
Time Frame: 5 month
|
To establish a correlation between sample matrices
|
5 month
|
|
Stability
Time Frame: 5 month
|
To determine sample stability with the NTproBNP2 Test Kit on the AQT90 FLEX analyzer
|
5 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 15, 2025
Primary Completion (Actual)
January 2, 2026
Study Completion (Actual)
January 2, 2026
Study Registration Dates
First Submitted
March 25, 2025
First Submitted That Met QC Criteria
March 25, 2025
First Posted (Actual)
April 1, 2025
Study Record Updates
Last Update Posted (Actual)
February 17, 2026
Last Update Submitted That Met QC Criteria
February 16, 2026
Last Verified
August 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- DC-087459
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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