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The Haemodynamic Effects of Mechanical Standard and Active Chest Compression-decompression During Out-of-hospital CPR

Not Applicable
Completed
Conditions
Cardiac Arrest
Interventions
Device: LUCAS2 AD
Registration Number
NCT02479152
Lead Sponsor
Physio-Control
Brief Summary

The aim of this randomized out-of-hospital cardiopulmonary resuscitation study is to investigate haemodynamics generated by the standard mechanical external chest compression device (LUCAS™ 2) compared to a new version generating chest compressions and active decompression above the initial starting position of the suction cup (LUCAS™ 2AD).

Detailed Description

Based on randomization patients will receive standard or active compression decompression chest compression and the haemodynamic effects will be compared.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
126
Inclusion Criteria
  • Unexpected adult out-of-hospital non-traumatic cardiac arrest where an attempt of resuscitation is considered appropriate in:
  • Patients 18 years or older
Exclusion Criteria
  • Traumatic cardiac arrest
  • Age believed to be less than 18 years
  • Known pregnancy
  • Victim not to be resuscitated (DNR orders)
  • Internals in prison
  • Included once in the study already
  • To Small/Large patients
  • Sustained ROSC occurring before the LUCAS™ 2 or LUCAS™ 2-AD can be applied to the patient, such that further CPR is not needed

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
LUCAS 2 ADLUCAS2 ADLUCAS 2 AD will be used for CPR
LUCAS2LUCAS2 ADLUCAS2 will be used for CPR
Primary Outcome Measures
NameTimeMethod
Hemodynamics measured as EtCO2During 30 minutes of CPR
Secondary Outcome Measures
NameTimeMethod
Intra arterial blood pressures,During 30 minutes of CPR
Oximetry,During 30 minutes of CPR
ROSC (Return of spontaneous circulation)During CPR
safetyDuring 30 minutes of CPR

Trial Locations

Locations (1)

Oslo University hospital

🇳🇴

Oslo, Norway

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