The Haemodynamic Effects of Mechanical Standard and Active Chest Compression-decompression During Out-of-hospital CPR
- 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
- Unexpected adult out-of-hospital non-traumatic cardiac arrest where an attempt of resuscitation is considered appropriate in:
- Patients 18 years or older
- 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
Group Intervention Description LUCAS 2 AD LUCAS2 AD LUCAS 2 AD will be used for CPR LUCAS2 LUCAS2 AD LUCAS2 will be used for CPR
- Primary Outcome Measures
Name Time Method Hemodynamics measured as EtCO2 During 30 minutes of CPR
- Secondary Outcome Measures
Name Time Method Intra arterial blood pressures, During 30 minutes of CPR Oximetry, During 30 minutes of CPR ROSC (Return of spontaneous circulation) During CPR safety During 30 minutes of CPR
Trial Locations
- Locations (1)
Oslo University hospital
🇳🇴Oslo, Norway