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

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

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00560248
Acronym
BEACON
Enrollment
1897
Registered
2007-11-19
Start date
2007-11-30
Completion date
2009-09-30
Last updated
2010-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Pain

Keywords

Chest Pain, STEMI, UA/NSTEMI, ACS, Emergency Department

Brief 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.

Detailed 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.

Interventions

None listed

Sponsors

Heartscape Technologies, Inc.
CollaboratorINDUSTRY
Novella Clinical
CollaboratorOTHER
PharmaVigilant
CollaboratorUNKNOWN
The Cleveland Clinic
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
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 diagnosisIndex hospitalization

Secondary

MeasureTime frame
Time to treatment, economic outcomes and survival outcomes1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026