NCT00641069

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2008

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 18, 2008

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 21, 2008

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2009

Completed
Last Updated

July 15, 2009

Status Verified

July 1, 2009

Enrollment Period

11 months

First QC Date

March 18, 2008

Last Update Submit

July 14, 2009

Conditions

Cardiac Arrest

Keywords

Cardiac arrestCardiopulmonary resuscitation

Outcome Measures

Primary Outcomes (1)

  • Diastolic blood pressures produced by manual and then by automated chest compressions will be recorded for each patient

    Instantaneously

Secondary Outcomes (2)

  • Systolic blood pressures produced by manual and then by automated chest compressions will be recorded for each patient

    Instantaneously

  • Mean blood pressures produced by manual and then by automated chest compressions will be recorded for each patient

    Instantaneously

Interventions

Automated load-distributing band deviceDEVICE

Blood pressure recording before and after starting up the automated band device

Also known as: AutoPulse™ 100, Zoll®

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients aged \> 18 with out-of-hospital cardiac arrest

You may qualify if:

  • Age ≥ 18
  • Refractory cardiac arrest

You may not qualify if:

  • Defective invasive arterial blood pressure monitoring

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital

Clichy, 92110, France

Location

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Francois-Xavier Duchateau, MD

    Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital

    PRINCIPAL INVESTIGATOR

  • Jean Mantz, MDPhD

    Departement of Anesthesiology, Intensive Care and EMS, Beaujon University Hospital

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 18, 2008

First Posted

March 21, 2008

Study Start

February 1, 2008

Primary Completion

January 1, 2009

Study Completion

January 1, 2009

Last Updated

July 15, 2009

Record last verified: 2009-07

Locations

FR(1)