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Are EMS Personnel Prepared to Identify and Decompression of Tension Pneumothorax

M

Medical University of Warsaw

Status

Unknown

Conditions

Tension Pneumothorax

Treatments

Device: ThoraQuik atraumatic set for pneumothorax decompression

Study type

Interventional

Funder types

Other

Identifiers

NCT02709122
02.010.1MR

Details and patient eligibility

About

The study aims to determine the level of knowledge and skills to recognize and decompression of tension pneumothorax

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

80 participants in 2 patient groups

With Tension pneumothorax
Experimental group
Description:
evaluation of the patient with the existing tension pneumothorax during a simulated CPR - breathing
Treatment:
Device: ThoraQuik atraumatic set for pneumothorax decompression
Without Tension pneumothorax
Experimental group
Description:
evaluation of the patient without the existing tension pneumothorax during a simulated CPR - breathing
Treatment:
Device: ThoraQuik atraumatic set for pneumothorax decompression

Trial contacts and locations

1

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Central trial contact

Lukasz Szarpak, PhD

Data sourced from clinicaltrials.gov

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