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Status unknownNCT02002481flightsUpdated May 5, 2015

Comparison of the Quality of CPR by Professional Helpers (Emergency Physicians / Paramedics) During Flights

An interventional study of transport in Cardiac Arrest, sponsored by University Hospital of Cologne. Status unknown at 1 site in Germany. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-05-05.

Sponsored by University Hospital of Cologne · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2015), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Investigation of the influence of narrowness and unusual circumstances on the CPR-quality

Read the detailed description

Even for paramedics and emergency physicians, the resuscitation of patients with cardiac arrest remains a challenge. Previous studies have shown that the cardiac output varies widely even under normal ambient conditions. Especially the mean frequenices of cardiac compression varies from 60 to 160/min, as well as the now-flow-time. Aim of this study is to investigate how narrowness and movement during a transport affect the CPR-performance.

For this, we examine the impact of the common transport options (air and ground) on the outcome-varity on a manikin. The subjects for this study are professional rescuers (emergency physicians / paramedics) who perform a 10 minute ALS-CPR in either normal circumstances (resuscitation-room) or during transportation.

02

Conditions studied

  • Cardiac Arrest

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03

In context

Heart Arrest

966 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's planned enrollment of 50 is below the median of 100 across 557 interventional studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

University Hospital of Cologne is the lead sponsor of 42 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • emergency physician
  • paramedic
  • > 18 years
  • \< 60 years

Exclusion criteria

Exclusion Criteria:

  • pregnant
  • lay rescuers
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • No intervention
    Control

    10 minutes ALS-CPR in a normal environment

  • Experimental
    Transport

    10 minutes ALS-CPR during a transport

    Other: transport

Interventions

  • Othertransport

    The manikin will be resuscitated during a transport in a vessel by a professional team (emergency physician / paramedic).

06

What researchers measure

Primary outcomes

  1. The average achieved cardiac output

    The main goal of the study is the average achieved cardiac output. Data acquisition is carried out on a resuscitation-manikin which can measure compression-rate (CR) and compression-depth (CD). The data are recorded by a computer during the CPR. To calculate the cardiac output, we multiply the average CR \[1/min\] with the average CD \[mm\] during the 10 min manikin-resuscitation. The thus obtained average cardiac-output (CO = CR x CD), measured in \[mm/min\], will be compared in each group.

    Time frame: after 10 minutes

Secondary outcomes

  1. Now-flow-time

    Second objective of the study is the time without chest-compression during the 10 minutes ALS-CPR. The now-flow-time is read out of the recorded manikin-data specify, in \[min\] and \[sec\]. As a result, the average now-flow-time in each group will be calculated and compared for each group.

    Time frame: after 10 minutes

07

Study locations

1 of 1 sites recruiting
  • Uniklinik Köln
    Köln, NRW 50937, Germany
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 5, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02002481
Lead sponsor
University Hospital of Cologne
Responsible party
Dr. med. Stefan Braunecker (Anesthesiologist, Researcher, University Hospital of Cologne) — Principal investigator
First posted
Dec 5, 2013
Start date
Dec 2013
Primary completion
Aug 2015 (estimated)
Completion
Dec 2015 (estimated)
Last update
May 5, 2015

Study contacts

Stefan Braunecker, MD
Contact
stefan.braunecker@uk-koeln.de
0221-478-97729
Jochen Hinkelbein, MD
Contact
jochen.hinkelbein@uk-koeln.de
0221-478-97729
Stefan Braunecker, MD
principal investigator · University Hospital Cologne
Jochen Hinkelbein, MD
principal investigator · University Hospital Cologne
Jan Hilgers, MD
principal investigator · University Hospital Cologne

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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