Ignite Creation Date:
2024-05-06 @ 10:11 AM
Last Modification Date:
2024-10-26 @ 12:26 PM
Study NCT ID:
NCT03194243
Status:
UNKNOWN
Last Update Posted:
2017-10-10
First Post:
2017-05-29
Brief Title:
Pathway and Urgent caRe of Dyspneic Patient at the Emergency Department in LorrainE District PURPLE
Sponsor:
Central Hospital Nancy France
Organization:
Central Hospital Nancy France
Study Overview
Official Title:
Pathway and Urgent caRe of Dyspneic Patient at the Emergency Department in LorrainE District
Status:
UNKNOWN
Status Verified Date:
2017-10
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PURPLE
Brief Summary:
This is an observational prospective multicenter study of patients admitted for acute dyspnea in an emergency department of the participating centers in the Lorraine district
The primary objective is to assess the outcome of this population according to the cause of acute dyspnea as well as identify the predictors of this outcome both overall and according to each acute dyspnea cause
The primary objective is to assess the outcome of this population according to the cause of acute dyspnea as well as identify the predictors of this outcome both overall and according to each acute dyspnea cause
Detailed Description:
This observational prospective multicenter study will be conducted using data from electronic medical records acquired as part of usual care in patients admitted for acute dyspnea in the emergency department Clinical treatment laboratory and imaging data acquired during the hospitalization in the emergency department and in the department that admitted the patients following the emergency department stay will be collected
Vital status will be recorded at 30 days and 1 year post-admission
Vital status will be recorded at 30 days and 1 year post-admission
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None