Observatory on Emergency Care for Acute Coronary Syndrome in Grand Est of France
NCT ID: NCT02887066
Last Updated: 2016-09-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
580 participants
OBSERVATIONAL
2014-09-30
2016-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Patients with thoracic pain and suspicion of ACS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* 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 with traumatic thoracic pain
* Patient with thoracic pain of parietal origin
* Patient with consciousness troubles
18 Years
ALL
No
Sponsors
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Central Hospital, Nancy, France
OTHER
Responsible Party
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Principal Investigators
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Tahar Chouihed
Role: PRINCIPAL_INVESTIGATOR
Service SAMU - SMUR - SAU, Hôpital Central, CHRU de Nancy
Other Identifiers
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2013/DAIICHI/CHEST-CHOUIHED/MS
Identifier Type: -
Identifier Source: org_study_id
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