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

Bradycardia Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02711748
• Other study ID #: 02.012.1MR
• Status: Recruiting
• Phase: N/A
• First received: February 22, 2016
• Last updated: March 16, 2016
• Start date: February 2016
• Est. completion date: March 2016

Study information

• Verified date: March 2016
• Source: Medical University of Warsaw
• Contact: Lukasz Szarpak, PhD
• Phone: +48500186225
• Email: lukasz.szarpak[@]gmail.com
• Is FDA regulated: No
• Health authority: Poland: Ministry of Science and Higher Education
• Study type: Interventional

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

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

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Bradycardia

Intervention

Device:
• electrostimulation
Electrostimulation using manual defibrillator
• cardiopulmonary resuscitation
CPR according to guidelines of European Resuscitation Council. Cardiopulmonary resuscitation using manual defibrillator

Locations

Country	Name	City	State
Poland	Medical University of Warsaw, Department of Emergency Medicine	Warsaw	Masovia

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of Warsaw

Country where clinical trial is conducted

Poland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	intraoperative	No
Secondary	Time to take proper action	time from rhythm interpretation to proper conduct	intraoperative	No