Comparison on the Efficacy of a Monophasic (AED)
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|ClinicalTrials.gov Identifier: NCT00472498|
Recruitment Status : Terminated (Terminated: No longer recruiting.)
First Posted : May 11, 2007
Last Update Posted : September 27, 2013
|Condition or disease|
The central purpose of this study is to compare the clinical outcomes of patients who suffered a cardiac arrest while hospitalized at the VA and were resuscitated after biphasic defibrillators were implemented in 2001 to clinical outcomes of patients who suffered cardiac arrest before 2001.
This study will retrospectively collect and analyze clinical data related to the Atlanta VA Medical Center, a member of the National Registry of Cardiopulmonary Resuscitation, to assess clinical parameters in cardiac arrest survivors.
This study focuses on collecting data retrospectively in regard to cardiac arrest patients to discern what factors are playing a role in patient survival after cardiac arrest. Such data will help hospitals and physicians to improve quality of care in patients at risk for cardiac arrest as well as to implement strategies to reduce such events or improve management of these high-risk patients in order to save lives.
|Study Type :||Observational|
|Actual Enrollment :||95 participants|
|Observational Model:||Case Control|
|Official Title:||Comparison on the Efficacy of a Monophasic, Manually Operated Defibrillator to That of a Biphasic Automatic External Defibrillator in the Hospital Setting.|
|Study Start Date :||June 2005|
|Primary Completion Date :||February 2007|
|Study Completion Date :||February 2007|
Patients resuscitated after 2001
Patients who suffer cardiac arrests after 2001.
- s who suffered a cardiac arrest while hospitalized at the VA and were resuscitated [ Time Frame: Information on patients who suffered cardiac arrest before 2001 ]
- This study is observational. [ Time Frame: Comparison before and after 2001 ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00472498
|Principal Investigator:||Samuel C Dudley, MD, PhD||Veterans Administration Medical Center|