Utility of Serial BNP Levels in Emergency Department CHF
The Utility of Serial BNP Levels as a Predictor of Adverse Outcomes in Emergency Department CHF
1 other identifier
observational
52
1 country
1
Brief Summary
The purpose of the study is to determine if a series of BNP blood tests performed on patients who present to the Emergency Department with congestive heart failure (CHF) can predict which patients may have adverse outcomes. If the BNP is shown to be predictive of bad outcomes in certain patients, those patients might receive more intensive therapy early to prevent such outcomes. This was a prospective trial enrolling patients who presented to the ED and were diagnosed with heart failure. Subjects had a blood test for BNP, which is elevated in the presence of heart failure, collected twelve hours after their initial clinical BNP was obtained in the ED. Demographics, history, length of hospital stay, and other approved data were collected. At 30 days and 6 months after discharge, a follow up call was made to determine if the subject had required additional emergency care, had been admitted to a hospital, or had died during that period of time.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Sep 2002
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2002
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2006
CompletedFirst Submitted
Initial submission to the registry
September 21, 2007
CompletedFirst Posted
Study publicly available on registry
September 24, 2007
CompletedSeptember 24, 2007
April 1, 2007
September 21, 2007
September 21, 2007
Conditions
Keywords
Study Arms (2)
Admitted
Patients presenting to the ED with acute exacerbation of CHF who require admission to the hospital directly from the ED
Observational
Patients who present to the ED for acute exacerbation of CHF who are transferred to the Observation Unit from the ED for up to 24 hours.
Eligibility Criteria
You may qualify if:
- age18 or older
- primary diagnosis of CHF in the Emergency Department
- admission to the hospital or transfer to the Observation Unit
You may not qualify if:
- minors, prisoners,pregnant women,unable to provide consent
- unstable angina or acute myocardial infarction in the ED
- dialysis dependent patients
- use of nesiritide as a therapy in the ED
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Ohio State University Medical Center
Columbus, Ohio, 43210, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Brian C Hiestand, MD
Ohio State University
Study Design
- Study Type
- observational
- Observational Model
- DEFINED POPULATION
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 21, 2007
First Posted
September 24, 2007
Study Start
September 1, 2002
Study Completion
June 1, 2006
Last Updated
September 24, 2007
Record last verified: 2007-04