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Clinical Trial Summary

The proposed study intends to evaluate the impact of the NT-proBNP assay on the diagnosis of heart failure in patients with dyspnea of unknown etiology presenting to the emergency room and admitted to the medical wards.


Clinical Trial Description

The proposed study intends to evaluate the impact of the NT-proBNP assay on the diagnosis of heart failure in patients with dyspnea of unknown etiology presenting to the emergency room and admitted to the medical wards.

Patients will be consented and randomized to open or blinded NT-proBNP test performed within 90 minutes in a venous blood sample.

Evaluation of the ER diagnosis and final discharge diagnosis in admitted patients will be carried out in light of the NT-proBNP results. ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00271128
Study type Observational
Source Hillel Yaffe Medical Center
Contact
Status Active, not recruiting
Phase N/A
Start date October 2005
Completion date September 2007

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