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

This study has been terminated.
(Loss of funding)
Sponsor:
Collaborators:
Heartscape Technologies, Inc.
Novella Clinical
PharmaVigilant
Information provided by:
The Cleveland Clinic
ClinicalTrials.gov Identifier:
NCT00560248
First received: November 16, 2007
Last updated: February 18, 2010
Last verified: February 2010

November 16, 2007
February 18, 2010
November 2007
September 2009   (final data collection date for primary outcome measure)
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 [ Time Frame: Index hospitalization ] [ Designated as safety issue: No ]
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. [ Time Frame: Index hospitalization ]
Complete list of historical versions of study NCT00560248 on ClinicalTrials.gov Archive Site
Time to treatment, economic outcomes and survival outcomes [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Time to treatment, economic outcomes and survival outcomes. [ Time Frame: 1 year ]
Not Provided
Not Provided
 
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

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.

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.

Observational
Observational Model: Case-Only
Time Perspective: Retrospective
Not Provided
Not Provided
Non-Probability Sample

Patients presenting to the Emergency Department with chest pain.

Chest Pain
Not Provided
I
Patients presenting to the Emergency Department with chest pain suspected to be of cardiac origin.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
1897
September 2009
September 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria:

  • None
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00560248
CCF2007-001, CCF2007-001
Yes
W. Frank Peacock, MD, Cleveland Clinic
The Cleveland Clinic
  • Heartscape Technologies, Inc.
  • Novella Clinical
  • PharmaVigilant
Principal Investigator: William F. Peacock, MD The Cleveland Clinic
Principal Investigator: Deepak L. Bhatt, MD VA Boston Healthcare System
Principal Investigator: Venugopal Menon, MD The Cleveland Clinic
The Cleveland Clinic
February 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP