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NT-proBNP for Evaluation of the Dyspneic Patient in the Emergency Room and the Medical Ward

NT-proBNP for Evaluation of the Dyspneic Patient in the Emergency Room and the Medical Ward (BNP4EVER)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00271128
Enrollment
500
Registered
2005-12-30
Start date
2005-10-31
Completion date
2007-09-30
Last updated
2008-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Exacerbation, Shortness of Breath

Keywords

NT-proBNP, Heart failure, Dyspnea

Brief 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.

Detailed 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.

Interventions

None listed

Sponsors

Hillel Yaffe Medical Center
Lead SponsorOTHER_GOV

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Acute shortness of breath of unknown etiology as presentation to the emergency room 2. Possible acute exacerbation of known heart failure

Exclusion criteria

None -

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026