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

NCT00271128 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2008-03-20

No results posted yet for this study

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.

Conditions

Sponsors & Collaborators

  • Hillel Yaffe Medical Center

    lead OTHER_GOV

Principal Investigators

  • Simcha R Meisel, MD MSc · Hillel Yaffe Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-10-31
Completion
2007-09-30

Countries

  • Israel

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00271128 on ClinicalTrials.gov