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

The Haemodynamic Effects of Mechanical Standard and Active External Chest Compression-decompression During Out-of-hospital Cardiopulmonary Resuscitation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02479152
Enrollment
126
Registered
2015-06-24
Start date
2015-04-30
Completion date
2017-04-30
Last updated
2017-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest

Keywords

Mechanical CPR, Hemodynamics

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.

Interventions

DEVICELUCAS2 AD

LUCAS™ 2AD with compressions like the standard LUCAS™ 2 but added decompressions above the initial start position.

Sponsors

GE Healthcare
CollaboratorINDUSTRY
Physio-Control
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Hemodynamics measured as EtCO2During 30 minutes of CPR

Secondary

MeasureTime frame
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

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026