Viewing Study NCT00641069


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Study NCT ID: NCT00641069
Status: COMPLETED
Last Update Posted: 2009-07-15
First Post: 2008-03-18
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Automated Chest Compression in Cardiac Arrest
Sponsor: Beaujon Hospital
Organization:

Study Overview

Official Title: Effect on Hemodynamics of Automated Band Chest Compression Device in Cardiac Arrest Resuscitation
Status: COMPLETED
Status Verified Date: 2009-07
Last Known Status: None
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: None
Brief Summary: To evaluate the effect of use of automated chest compression device on blood pressure in patients presenting with cardiac arrest. Higher systolic, diastolic and mean blood pressures are expected.
Detailed Description: The protocol compares arterial pressures produced by an automated self-adjusting load-distributing band device (AutoPulseā„¢ 100, ZollĀ®) with those of manual cardiopulmonary resuscitation in refractory out-of-hospital cardiac arrest. Each patient will receive first manual compressions and then automated resuscitation.

Patients presenting with cardiac arrest are treated following standard advanced life support guidelines. They are intubated and ventilated, received epinephrine and defibrillation if appropriate. Manuel chest compressions are continued. An arterial catheter is placed to monitor hemodynamics continuously as we usually do in this case. Patients are included at this stage. Three blood pressure values (every 1 minutes) are recorded. Then, the automated band device is started up without any pause, following our procedure for refractory cardiac arrest. Three blood pressure values are recorded again, during automated cardiopulmonary resuscitation.

Study Oversight

Has Oversight DMC: False
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?: