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Sponsored by: |
Hillel Yaffe Medical Center |
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Information provided by: | Hillel Yaffe Medical Center |
ClinicalTrials.gov Identifier: | NCT00271128 |
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.
Condition |
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Shortness of Breath Acute Exacerbation |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | NT-proBNP for Evaluation of the Dyspneic Patient in the Emergency Room and the Medical Ward (BNP4EVER) |
Estimated Enrollment: | 500 |
Study Start Date: | October 2005 |
Estimated Study Completion Date: | September 2007 |
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.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
None -
Study ID Numbers: | hymc34/2005 |
Study First Received: | December 29, 2005 |
Last Updated: | March 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00271128 |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
NT-proBNP Heart failure Dyspnea |
Signs and Symptoms Heart Failure Respiratory Tract Diseases Respiration Disorders |
Signs and Symptoms, Respiratory Emergencies Dyspnea |
Disease Attributes Pathologic Processes |