Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06608771
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-08
Brief Title:
Outcome of Cardiac Arrest Patients Following Guidelines Implementation Over the Years
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Implementation of the New Guidelines on the Management of Patients Resuscitated From Cardiac Arrest and Impact on Survival a Multicenter Retrospective Observational Study
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
IMPACT-ACC
Brief Summary:
The study aims to evaluate the level of local implementation of the new interventions introduced by the guidelines for post-cardiac arrest management and their impact on the survival of patients resuscitated from cardiac arrest and admitted to intensive care over a 14-year period During this time period the European Resuscitation Council ERC and the European Society of Intensive Care Medicine ESICM introduced three new guidelines for post-cardiac arrest management each five years apart the 2010 2015 and 2021 guidelines
Detailed Description:
This study is a retrospective multicenter cohort observational study two centers involved Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico and Fondazione IRCCS San Gerardo dei Tintori
All patients admitted to the Intensive Care Units ICU of the hospitals involved in the study from January 1 2011 to May 30 2024 following cardiac arrest of any etiology who meet the inclusion and exclusion criteria will be enrolled
All patients admitted to the Intensive Care Units ICU of the hospitals involved in the study from January 1 2011 to May 30 2024 following cardiac arrest of any etiology who meet the inclusion and exclusion criteria will be enrolled
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None