Trial Information

Summary: A Study of NT-Pro Brain Natriuretic Peptide (NT-proBNP) in Patients Presenting With Acute Dyspnea.

Status: Completed

Protocol Number: CAN0010

Sponsor:

Company Division: Diagnostic

Official Scientific Title: The 'improved management of patients with congestive heart failure in Canada (IMPROVE-CHF CANADA)' study.

Brief Summary: This study will evaluate the use of plasma NT-proBNP measurements to improve the diagnostic accuracy of congestive heart failure (CHF) and the prediction of clinical outcomes in patients who present to emergency departments with acute dyspnea. Patients will be randomized to a conventional care group, or to conventional care plus measurement of plasma NT-proBNP.

Study Phase: N/A

Study Design / Study Details:

  • Purpose:
  • Allocation: Randomized
  • Masking: Double Blind
  • Control:
  • Assignment: Parallel
  • Endpoints:

Study Type:

Interventional

Condition: Congestive Heart Failure

Intervention Type: Diagnostic Test

Intervention Name: ELECSYS®proBNP

Primary Outcome:

Key Secondary Outcomes:

Inclusion Criteria:

  • adult patients, >=18 years of age;
  • presenting to emergency department with shortness of breath, of suspected cardiac etiology.

Exclusion Criteria:

  • dyspnea clearly not due to CHF;
  • acute myocardial infarction;
  • advanced renal failure.

 

Gender: Males or Females

Age Limits: Min: 18 Years

Accepts Healthy Volunteers: No

Anticipated Start Date: December, 2004

Trial Registration Date: 11/23/2006

Date Last Updated: 12/08/2006

Link To Trial Results

Contact:

Research Site:
Located In:
Calgary, AB, Canada, T2N 4N2
Telephone: 973-235-5000 or 800-526-6367

 

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Trial listings updated: September 2, 2008 at 1:51:09 PM


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