Trial Information
Summary: PROMPT study: A study of NT-proBNP in an emergency setting
Status: Completed
Protocol Number: 21103
Sponsor: Roche Diagnostics Germany GmbH
Company Division: Diagnostic
Official Scientific Title: Usefulness of NT-proBNP in the internal emergency department [PROMPT]
Brief Summary: This study will investigate the value of NT-proBNP in the management of patients presenting in the emergency department or in the chest pain unit. The influence of the determination of the NT-proBNP value on diagnostic decision-making, and further diagnostic and therapeutic procedures, will be evaluated.
Study Phase: N/A
Study Design / Study Details:
- Purpose:
- Allocation: Randomized
- Masking: Open Label
- Control: Placebo
- Assignment: Parallel
- Endpoints:
Study Type:
Interventional
Condition: Heart Disease
Intervention Type: Diagnostic Test
Intervention Name: proBNP RP Elecsys Kit
Primary Outcome:
Key Secondary Outcomes:
Inclusion Criteria:
- patients ≥ 65 years of age;
- presenting to the internal emergency room or chest pain unit;
- informed consent.
Exclusion Criteria:
- unambiguously clear symptoms allowing clinician to make decisions without further diagnostic testing.
Gender: Males or Females
Age Limits: Min: 65 Years
Accepts Healthy Volunteers: No
Anticipated Start Date: January, 2006
Trial Registration Date: 05/11/2006
Date Last Updated: 02/07/2008
Link To Trial Results
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Contact:
Research Site:
Located In:
Munich, Germany,
Telephone: 973-235-5000 or 800-526-6367
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Trial listings updated: November 17, 2008 at 2:29:19 PM