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NCT00560248 Clinical Trial

The BEACON Registry: Best Expert Agreement for Care of Occult Myocardial Infarction (MI) Nationally

Chest Pain Clinical Trial

— BEACON  

Official title:
The BEACON Registry: Best Expert Agreement for Care of Occult MI Nationally

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00560248
Other study ID # CCF2007-001
Secondary ID CCF2007-001
Status Terminated
Phase N/A
First received November 16, 2007
Last updated February 18, 2010
Start date November 2007
Est. completion date September 2009

Study information
Verified date February 2010
Source The Cleveland Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this registry is to assess and improve the process of care and health outcomes of patients presenting to the Emergency Department with chest pain suspected to be of cardiac origin. The study will identify which methods facilitate the diagnosis and risk stratification of ST elevation myocardial infarction (STEMI) or non STEMI, including patients with occult myocardial infarction (MI), and result in a shorter time to definitive diagnosis and treatment.

Description:

The BEACON Registry is a multi-center data collection and follow-up registry. Participating Sites will collect information on patients presenting to the Emergency Department (ED) with chest pain. The purpose of the BEACON Registry is to evaluate the impact of new technologies, practice patterns and initiatives on patient time to diagnosis, patient time to treatment, patient survival and overall economics.

Recruitment information / eligibility
Status Terminated
Enrollment 1897
Est. completion date September 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients presenting with chest pain suspected to be of cardiac origin.

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Cleveland Clinic Cleveland Ohio

Sponsors (4)
Lead Sponsor Collaborator
The Cleveland Clinic Heartscape Technologies, Inc., Novella Clinical, PharmaVigilant

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Time to definitive diagnosis of STEMI, UA/NSTEMI and non-cardiac chest pain; time to disposition decision will be used as an objective measure of time to definitive diagnosis Index hospitalization No
Secondary Time to treatment, economic outcomes and survival outcomes 1 year No
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