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Comparison of the Quality of CPR by Lay Rescuers With and Without Feedback Devices

NCT ID: NCT02000505

Last Updated: 2015-05-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

240 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-11-30

Study Completion Date

2016-02-29

Brief Summary

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Comparison of various methods to improve the quality of CPR

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Detailed Description

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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 among professional helpers. This is especially due to some very different mean frequencies of cardiac compression wich vary from 60 to 160/min for paramedics. Aim of this study is to investigate whether the use of feedback-devices during cardiac-pulmonary resuscitation (CPR) can lead to an improvement of the cardiac output and may improve survival.

For this, we examine the impact of different feedback-methods on the frequence-variety on manikin by lay rescuers. Overall, we compare three different devices for feedback during CPR. The subjects for this study are lay rescuers who perform a 5 minute chest-compression-only CPR.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Control

5 minutes chest-compression-only CPR, without any support

Group Type NO_INTERVENTION

No interventions assigned to this group

PocketCPR

5 minutes chest-compression-only CPR, with support

Group Type EXPERIMENTAL

PocketCPR

Intervention Type DEVICE

5 minutes chest-compression-only CPR, using Zoll PocketCPR

Metronome

5 minutes chest-compression-only CPR, with support

Group Type EXPERIMENTAL

Metronome

Intervention Type DEVICE

5 minutes chest-compression-only CPR, using a metronome

110bpm Song

5 minutes chest-compression-only CPR, with support

Group Type EXPERIMENTAL

110bpm Song

Intervention Type DEVICE

5 minutes chest-compression-only CPR, using a song with 110bpm for support

Interventions

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PocketCPR

5 minutes chest-compression-only CPR, using Zoll PocketCPR

Intervention Type DEVICE

Metronome

5 minutes chest-compression-only CPR, using a metronome

Intervention Type DEVICE

110bpm Song

5 minutes chest-compression-only CPR, using a song with 110bpm for support

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* lay rescuers
* \>18 years
* \<60 years

Exclusion Criteria

* professional rescuers
* pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital of Cologne

OTHER

Sponsor Role lead

Responsible Party

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Dr. med. Stefan Braunecker

Anesthesiologist, Researcher

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Stefan Braunecker, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Cologne

Jochen Hinkelbein, MD

Role: STUDY_DIRECTOR

University Hospital Cologne

Locations

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Uniklinik Köln

Cologne, , Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Stefan Braunecker, MD

Role: CONTACT

[email protected]

Facility Contacts

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Stefan Braunecker, MD

Role: primary

[email protected]
0221-478-97729

Other Identifiers

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10-333

Identifier Type: -

Identifier Source: org_study_id

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