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

P

Physio-Control

Status

Completed

Conditions

Cardiac Arrest

Treatments

Device: LUCAS2 AD

Study type

Interventional

Funder types

Industry

Identifiers

NCT02479152
Protocol ID 11, March 2015

Details and patient eligibility

About

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).

Full description

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

Enrollment

126 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

126 participants in 2 patient groups

LUCAS 2 AD
Active Comparator group
Description:
LUCAS 2 AD will be used for CPR
Treatment:
Device: LUCAS2 AD
LUCAS2
Other group
Description:
LUCAS2 will be used for CPR
Treatment:
Device: LUCAS2 AD

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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