NCT00560248

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,897

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2007

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2007

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

November 16, 2007

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 19, 2007

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2009

Completed
Last Updated

February 22, 2010

Status Verified

February 1, 2010

Enrollment Period

1.8 years

First QC Date

November 16, 2007

Last Update Submit

February 18, 2010

Conditions

Chest Pain

Keywords

Chest PainSTEMIUA/NSTEMIACSEmergency Department

Outcome Measures

Primary Outcomes (1)

  • 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

Secondary Outcomes (1)

  • Time to treatment, economic outcomes and survival outcomes

    1 year

Study Arms (1)

I

Patients presenting to the Emergency Department with chest pain suspected to be of cardiac origin.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients presenting to the Emergency Department with chest pain.

You may qualify if:

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

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Location

MeSH Terms

Conditions

Chest PainST Elevation Myocardial InfarctionEmergencies

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMyocardial InfarctionMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesNecrosisDisease Attributes

Study Officials

  • 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

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

November 16, 2007

First Posted

November 19, 2007

Study Start

November 1, 2007

Primary Completion

September 1, 2009

Study Completion

September 1, 2009

Last Updated

February 22, 2010

Record last verified: 2010-02

Locations

US(1)