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Observatory on Emergency Care for Acute Coronary Syndrome in Grand Est of France

Observatory on Emergency Care for Acute Coronary Syndrome in Grand Est of France

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02887066
Acronym
CHEST
Enrollment
580
Registered
2016-09-01
Start date
2014-09-30
Completion date
2016-09-30
Last updated
2016-09-07

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

Conditions

Acute Coronary Syndrome

Brief summary

The purpose is to build up a data observatory of individuals with thoracic pain evoking acute coronary syndrome (ACS). The aim is the characterization of this population of patients consulting at emergency department, the evaluation of therapeutic strategies with regard to guidelines and the becoming of patients including severe complications and mortality.

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Resident in Grand Est of France (Lorraine, Champagne Ardenne) under medical care at the emergency room or outside of hospital or in cardiology: * Outside of hospital: for thoracic or epigastric pain with suspicion of ACS Emergency: for thoracic pain for which the doctor will prescribe troponin or troponin kinetics * Affiliation to social security

Exclusion criteria

* Patient affected by ACS with ST segment elevation * Patient with traumatic thoracic pain * Patient with thoracic pain of parietal origin * Patient with consciousness troubles

Design outcomes

Primary

MeasureTime frame
Mortality30 days
Severe complications30 days
Benefit/risk ratio of treatmentsday 0

Outcome results

None listed

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