Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Out of Hospital Cardiac Arrest
  • Pulmonary Ventilation
Type
Observational
Design
Observational Model: Case-OnlyTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The inclusion is estimated to run over a two-year period to reach the goal of at least 200 patients. The study has been preceded by a trial period in an effort to solve any logistic and technical problems. The study will be a prospective descriptive multicenter study where measurement of ventilation...

The inclusion is estimated to run over a two-year period to reach the goal of at least 200 patients. The study has been preceded by a trial period in an effort to solve any logistic and technical problems. The study will be a prospective descriptive multicenter study where measurement of ventilation data will be sampled during CPR by EMS treating patients with OHCA. Any results from standard laboratory tests related to ventilation quality will be retracted from the patient medical journal systems. In addition to ventilatory variables measured as endpoints, secondary endpoints will also be outcome measures as any ROSC, survival and neurological outcome (mRS, GOS-E) measured at 30 days and at 6 months.

Tracking Information

NCT #
NCT04237727
Collaborators
Regionale Ambulance Voorziening, Amersfoort, Utrecht, Netherlands
Investigators
Principal Investigator: Sten Rubertsson, PhD Uppsala University department of surgical sciences Study Chair: David Smekal, PhD Uppsala University department of surgical sciences Study Chair: Johan Mällberg, BsSC Uppsala University department of surgical sciences Study Chair: René Boomars, MSc Regionale Ambulance Voorziening Utrecht (RAVU) Study Chair: Thijs Verhagen, MD Regionale Ambulance Voorziening Utrecht (RAVU)