BNP Therapy Observation Unit Outcomes STudy (BOOST)
Stopped early · Phase 4
Conditions studied: Congestive Heart Failure
In brief
The investigators hypothesize that patients admitted to an emergency department (ED) observation unit will have a decreased rate of hospital admissions and ED recidivism when treated with nesiritide versus standard therapy. The investigators also hypothesize that decreasing B-type Natriuretic Peptide (BNP) levels during treatment in an ED observation unit will predict improved patient outcomes.
Key facts
- Study ID
- NCT00453453
- Run by
- Emory University
- People needed
- 17
- Starts
- 2007-03-01
- Expected to finish
- 2007-09-01
- Last updated by the study team
- 2015-02-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patient > 18 years of age
- Have a working diagnosis of HF, as determined by the emergency physician using the Boston Criteria. A score of 8-12 is required for inclusion in the study.
- Alert, oriented and able to provide informed consent.
- Able to be contacted by telephone for follow up after discharge, and have none of the study exclusion criteria.
You may not qualify if…
- Dialysis Dependent Renal Failure
- Temperature > 38.5 degrees celsius
- Pneumonia (Infiltrates on Chest X-ray)
- Requiring IV vasoactive agents (Other than Nesiritide)
- Killip Class III/IV
- Systolic blood pressure < 90 mmHg
- EKG diagnostic or suggestive of Acute myocardial infarction or ischemia
- Abnormal Cardiac Markers
- Lack of a telephone
- Inability to provide informed consent due to cognitive impairment or a severe psychiatric disorder
Where it is running
- Grady Memorial Hosptial — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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