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

Primary Purpose

Bradycardia

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
electrostimulation
cardiopulmonary resuscitation
Sponsored by
Medical University of Warsaw
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bradycardia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Medical University of Warsaw, Department of Emergency MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Bradycardia

PEA

Arm Description

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

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

Outcomes

Primary Outcome Measures

Questionnaire to assess effectiveness of the rhythm recognition and participants' knowledge on life-threatening rhythms
The effectiveness of the rhythm recognition. participants knowledge on life-threatening rhythms

Secondary Outcome Measures

Time to take proper action
time from rhythm interpretation to proper conduct

Full Information

First Posted
February 22, 2016
Last Updated
March 16, 2016
Sponsor
Medical University of Warsaw
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1. Study Identification

Unique Protocol Identification Number
NCT02711748
Brief Title
Can Medical Personnel Properly Proceed in the Case of a Patient With Bradycardia?
Official Title
Can Medical Personnel Properly Proceed in the Case of a Patient With Bradycardia?
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2016 (undefined)
Primary Completion Date
March 2016 (Anticipated)
Study Completion Date
March 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Warsaw

4. Oversight

Data Monitoring Committee
No

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bradycardia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bradycardia
Arm Type
Experimental
Arm Description
Treatment In case of bradycardia. The patient unconscious, breathing preserved in ECG - bradycardia 40 / min with pulse.
Arm Title
PEA
Arm Type
Experimental
Arm Description
In case of bradycardia. The patient unconscious, not breathing, the ECG - bradycardia 30 / min - no pulse. Pulseless electrical activity
Intervention Type
Device
Intervention Name(s)
electrostimulation
Intervention Description
Electrostimulation using manual defibrillator
Intervention Type
Device
Intervention Name(s)
cardiopulmonary resuscitation
Intervention Description
CPR according to guidelines of European Resuscitation Council. Cardiopulmonary resuscitation using manual defibrillator
Primary Outcome Measure Information:
Title
Questionnaire to assess effectiveness of the rhythm recognition and participants' knowledge on life-threatening rhythms
Description
The effectiveness of the rhythm recognition. participants knowledge on life-threatening rhythms
Time Frame
intraoperative
Secondary Outcome Measure Information:
Title
Time to take proper action
Description
time from rhythm interpretation to proper conduct
Time Frame
intraoperative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lukasz Szarpak, PhD
Phone
+48500186225
Email
lukasz.szarpak@gmail.com
Facility Information:
Facility Name
Medical University of Warsaw, Department of Emergency Medicine
City
Warsaw
State/Province
Masovia
ZIP/Postal Code
02-005
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lukasz Szarpak, PhD
Phone
+48500186225
Email
lukasz.szarpak@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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

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