Can Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation Improve Survival of out-of Hospital Cardiac Arrest?
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02010151|
Recruitment Status : Recruiting
First Posted : December 12, 2013
Last Update Posted : January 17, 2018
|Condition or disease||Intervention/treatment||Phase|
|Out of Hospital Cardiac Arrest||Other: NAD-CPR||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||3776 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Population Based Intervention Trial of Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation|
|Study Start Date :||March 2015|
|Estimated Primary Completion Date :||December 2018|
|Estimated Study Completion Date :||December 2018|
When dispatcher detects a patient with OHCA, the dispatcher activates trained neighborhoods by informing events nearby using short message service via cellular phone. The neighborhood within geographically accessible area who could perform effective CPR and defibrillation would be alerted with event of OHCA and the nearest AED.
When Dispatcher detects OHCA, short message service (SMS)about the OHCA event and information about the location of nearest AED is sent to trained laypersons within geographically accessible area.
No Intervention: Conventional dispatcher assisted CPR
When dispatcher detects OHCA, they instruct the caller with CPR instructions. This is conventional dispatcher assisted CPR performed in Seoul.
- Survival to discharge [ Time Frame: 40 months ]difference of survival to discharge rate of before intervention period (20 months) and intervention period (20 months)
- Pre-hospital return of spontaneous circulation (ROSC) [ Time Frame: 40 months ]difference of pre-hospital ROSC rate of before intervention period (20 months)and intervention period (20 months)
- survival to admission [ Time Frame: 40 months ]difference of survival to admission rate of before intervention period (20 months)and intervention period (20 months)
- good neurological recovery [ Time Frame: 40 months ]Cerebral performance category 1 or 2 is defined as good neurological recovery. Secondary outcome is difference of good neurological recovery rate of before intervention period (20 months)and intervention period (20 months).
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): NCT02010151
|Contact: Soyeon Kong, PhDemail@example.com|
|Korea, Republic of|
|Seoul Metropolitan City||Recruiting|
|Seoul, Korea, Republic of|
|Sub-Investigator: Kyoung Jun Song, MD|
|Sub-Investigator: Eui Jung Lee, MD|
|Sub-Investigator: Joo Yeong Kim, MD|
|Sub-Investigator: Yu Jin Lee, MD|
|Sub-Investigator: Ju Ok Park, MD|
|Sub-Investigator: Ki Jeong Hong, MD|
|Sub-Investigator: So Young Ha, MD|
|Sub-Investigator: Kwang Soo Bae, MD|
|Sub-Investigator: Jeong Eun Kim, MPH|
|Principal Investigator:||Sang Do Shin, MD, PhD||Seoul National University Hospital|