Single-rescuer Pediatric Resuscitation (SRPR)

Medical University of Warsaw

Status: Completed

Conditions: Chest Compression

Treatments: Other: Manually chest compressions; Device: LifeLine ARM; Device: Cardiopump

Study type: Interventional

Funder types: Other

Identifiers

NCT02694900

02.009.1MR

Details and patient eligibility

About

The objective of this pilot study was to compare the manual chest compressions (CC) versus CC feedback device TrueCPR vs mechanical CC device LifeLine ARM during simulated pediatric cardiopulmonary resuscitation

Enrollment: 52 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• give voluntary consent to participate in the study
• maximum 1 year of work experience in medicine
• minimum 10 clinical resuscitations
• paramedics, nurses, physicians

Exclusion criteria

• not meet the above criteria
• wrist or low back diseases
• pregnancy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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52 participants in 2 patient groups

Resuscitation on the flor

Experimental group

Description:

2 min asynchronous cardiopulmonary resuscitation. The patient lies on the floor

Treatment:

Device: LifeLine ARM

Device: Cardiopump

Other: Manually chest compressions

Resuscitation on the stretcher

Experimental group

Description:

2 min asynchronous cardiopulmonary resuscitation. The patient lies on a stretcher

Treatment:

Device: LifeLine ARM

Device: Cardiopump

Other: Manually chest compressions