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

Acute Coronary Syndrome Clinical Trial

— CHEST  

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02887066
• Other study ID #: 2013/DAIICHI/CHEST-CHOUIHED/MS
• Status: Active, not recruiting
• Phase: N/A
• First received: August 19, 2016
• Last updated: September 6, 2016
• Start date: September 2014
• Est. completion date: September 2016

Study information

• Verified date: August 2016
• Source: Central Hospital, Nancy, France
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Commission nationale de l'informatique et des libertés
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 580
• Est. completion date: September 2016
• Est. primary completion date: September 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Emergencies
• Syndrome

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Central Hospital, Nancy, France

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality		30 days	No
Primary	Mortality		1 year	No
Primary	Severe complications		30 days	No
Primary	Severe complications		1 year	No
Primary	Benefit/risk ratio of treatments		day 0	No
Primary	Benefit/risk ratio of treatments		30 days	No
Primary	Benefit/risk ratio of treatments		1 year	No