- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00641069
Automated Chest Compression in Cardiac Arrest
Effect on Hemodynamics of Automated Band Chest Compression Device in Cardiac Arrest Resuscitation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The protocol compares arterial pressures produced by an automated self-adjusting load-distributing band device (AutoPulse™ 100, Zoll®) 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 Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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Clichy, France, 92110
- Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age ≥ 18
- Refractory cardiac arrest
Exclusion Criteria:
- Defective invasive arterial blood pressure monitoring
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Diastolic blood pressures produced by manual and then by automated chest compressions will be recorded for each patient
Time Frame: Instantaneously
|
Instantaneously
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Systolic blood pressures produced by manual and then by automated chest compressions will be recorded for each patient
Time Frame: Instantaneously
|
Instantaneously
|
Mean blood pressures produced by manual and then by automated chest compressions will be recorded for each patient
Time Frame: Instantaneously
|
Instantaneously
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Francois-Xavier Duchateau, MD, Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital
- Study Chair: Jean Mantz, MDPhD, Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAND V6
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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