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CompletedNCT00587938Updated Jan 8, 2008

BNP Measurement Reduces Resource Utilization for Patients With CHF Admitted Thorough the ED

An observational study in Congestive Heart Failure, sponsored by Mayo Clinic. Completed at 1 site in United States. Open to participants aged 65 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2008-01-08.

Sponsored by Mayo Clinic · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
65 Years and older
Sex
All
01

Study summary

Measurement of brain natriuretic peptide (BNP) in dyspneic patients increases diagnostic accuracy for congestive heart failure (CHF). Limited information is available regarding economic outcomes attributable to BNP assay. The aim of this study was to assess the economic impact of BNP assay in elderly dyspneic patients presenting to the emergency department (ED).

Read the detailed description

Dyspneic patients 65 years were enrolled in a randomized, controlled trial; hemodynamically unstable patients were excluded. BNP (Biosite assay) levels were measured prior to physician assessment with randomization in 1:1 ratio to either BNP 1) level reported or 2) level not reported. ED physicians made triage decisions guided by clinical judgment and nomogram to aid in interpretation of BNP level. Primary outcome was mean total hospital cost per subject. Secondary outcomes included admission rate, service assignment, discharge diagnosis and length of stay. Differences between groups were compared by t-test with bootstrap. Costs reflect 2005 constant dollars.

02

Conditions studied

  • Congestive Heart Failure

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Keywords

  • congestive heart failure
  • Brain naturietic peptide
  • hospital utilization cost
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's enrollment of 200 is close to the median of 200 across 1,679 observational studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Dyspneic patients:65 years or older presenting to the ED with chief complaint of shortness of breath, were enrolled in a randomized, controlled trial.

Inclusion criteria

  • Dyspneic patients 65 years or older presenting to the ED with chief complaint of shortness of breath.

Exclusion criteria

Exclusion Criteria:

  • hemodynamically unstability
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (actual)
Biospecimen retention
Samples without dna

Groups and cohorts

  • A

    BNP level from protocol blood tests initiated in the ED, reported to ED physician prior to ED disposition.

  • B

    BNP level from protocol blood tests initiated in the ED, NOT reported to ED physician prior to ED disposition.

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What researchers measure

Primary outcomes

  1. Mean total hospital cost per subject

    Time frame: spans from ED eval through hospitalization discharge

Secondary outcomes

  1. Included admission rate, service assignment, discharge diagnosis, and length of stay.

    Time frame: from ED evaluation through hospitalization discharge

07

Study locations

1 site
  • Saint Marys Hospital, Mayo Clinic
    Rochester, Minnesota 55905, United States
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References and documents

Publications

  • Schmidt TA, Salo D, Hughes JA, Abbott JT, Geiderman JM, Johnson CX, McClure KB, McKay MP, Razzak JA, Schears RM, Solomon RC; SAEM Ethics Committee. Confronting the ethical challenges to informed consent in emergency medicine research. Acad Emerg Med. 2004 Oct;11(10):1082-9. doi: 10.1197/j.aem.2004.05.028. PubMed 15466152 ↗
  • Clavell AL, Stingo AJ, Aarhus LL, Burnett JC Jr. Biological actions of brain natriuretic peptide in thoracic inferior vena caval constriction. Am J Physiol. 1993 Dec;265(6 Pt 2):R1416-22. doi: 10.1152/ajpregu.1993.265.6.R1416. PubMed 8285286 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00587938
Lead sponsor
Mayo Clinic
First posted
Jan 8, 2008
Start date
Dec 2003
Primary completion
Mar 2005
Completion
Mar 2005
Last update
Jan 8, 2008

Study contacts

Raquel M Schears, MD, MPH
principal investigator · Mayo Clinic
Alfredo L Clavell, MD
principal investigator · Mayo Clinic
Lyle J Olsen, MD
study chair · Mayo Clinic
Paula J Santrach, MD
study director · Mayo Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2007. You cannot join it, but the record below documents what was studied.

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