Can Medical Personnel Properly Proceed in the Case of a Patient With Bradycardia?

NCT ID: NCT02711748

Last Updated: 2016-03-17

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

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-29

Study Completion Date

2016-03-31

Brief Summary

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The study aims to assess the regularity of the proceedings in the case of a patient with bradycardia ECG.

Detailed Description

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Conditions

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Bradycardia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Bradycardia

Treatment In case of bradycardia. The patient unconscious, breathing preserved in ECG - bradycardia 40 / min with pulse.

Group Type EXPERIMENTAL

electrostimulation

Intervention Type DEVICE

Electrostimulation using manual defibrillator

PEA

In case of bradycardia. The patient unconscious, not breathing, the ECG - bradycardia 30 / min - no pulse. Pulseless electrical activity

Group Type EXPERIMENTAL

cardiopulmonary resuscitation

Intervention Type DEVICE

CPR according to guidelines of European Resuscitation Council. Cardiopulmonary resuscitation using manual defibrillator

Interventions

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electrostimulation

Electrostimulation using manual defibrillator

Intervention Type DEVICE

cardiopulmonary resuscitation

CPR according to guidelines of European Resuscitation Council. Cardiopulmonary resuscitation using manual defibrillator

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* give voluntary consent to participate in the study
* maximum 1 year of work experience in medicine
* paramedics, nurses, physicians

Exclusion Criteria

* not meet the above criteria
* wrist or low back diseases
* pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medical University of Warsaw

OTHER

Sponsor Role lead

Responsible Party

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Ɓukasz Szarpak

Lukasz Szarpak

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medical University of Warsaw, Department of Emergency Medicine

Warsaw, Masovia, Poland

Site Status RECRUITING

Countries

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Poland

Central Contacts

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Lukasz Szarpak, PhD

Role: CONTACT

+48500186225

Facility Contacts

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Lukasz Szarpak, PhD

Role: primary

+48500186225

Other Identifiers

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02.012.1MR

Identifier Type: -

Identifier Source: org_study_id

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