Cardiac Arrest, Out-Of-Hospital Clinical Trial
Official title:
Doppler Ultrasound Pulse Detection in Out-of-Hospital Cardiac Arrest Patients: A Feasibility Study.
NCT number | NCT06249893 |
Other study ID # | 1549/2023 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 4, 2024 |
Est. completion date | April 30, 2024 |
The goal of this prospective observational study is to investigate the feasibility of using doppler point-of-care ultrasound on the femoral artery with a portable device to assess the presence of a pulse in patients suffering from cardiac arrest in the out-of-hospital environment. The main question is how often researchers are successful in acquiring the necessary ultrasound signal in the out-of-hospital environment.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | April 30, 2024 |
Est. primary completion date | March 31, 2024 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Out-of-hospital cardiac arrest treated by EMS - Minimum age of 18 years Exclusion Criteria: - Pregnancy or suspected pregnancy - Disapproval of the treating EMS team - Adults under legal guardianship - Inability to perform femoral artery doppler ultrasound due to limited access to the patient and possible interference with the treating EMS team - Inability to perform femoral artery doppler ultrasound due to injuries or anatomic abnormalities in the femoral region or necessary emergent medical interventions in the femoral region - Decision to transfer the patient to the hospital with ongoing CPR for emergent procedures such as extracorporeal CPR before femoral artery doppler ultrasound could be attempted - Inability to safely perform femoral artery doppler ultrasound due to environmental hazards |
Country | Name | City | State |
---|---|---|---|
Austria | Emergency Medical Service of Vienna | Vienna |
Lead Sponsor | Collaborator |
---|---|
Medical University of Vienna | Emergency Medical Service of Vienna, Ludwig Boltzmann Institute Digital Health and Patient Safety |
Austria,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility of femoral artery doppler ultrasound | If an ultrasound image of the femoral artery of sufficient quality for Doppler ultrasound can be obtained, the primary outcome will be considered to be positive. | During cardiac arrest, up to 45 minutes | |
Secondary | Time until ultrasound signal acquisition | The time until successful acquisition of the doppler ultrasound signal will be measured in 2-minute CPR-intervals and 30-second intervals (e.g. second CPR-interval, first 30 seconds). | During cardiac arrest, up to 45 minutes | |
Secondary | Discordance between doppler ultrasound and manual pulse checks. | The presence of a doppler ultrasound flow signal during rhythm analysis and the result of the manual pulse check that is performed in parallel by the treating EMS team will be evaluated and analyzed for discordance. | During cardiac arrest, up to 45 minutes | |
Secondary | Correlation of the result of manual pulse checks with doppler peak systolic velocity | The correlation of the result of manual pulse checks performed by the treating EMS team with the peak systolic velocity measured by doppler ultrasound will be analyzed. | During cardiac arrest, up to 45 minutes | |
Secondary | Patient factors influencing probability of successful doppler ultrasound image acquisition | Patient factors sex, age, approximated bodyweight and suspected cause of cardiac arrest will be analyzed for correlation with successful doppler ultrasound image acquisition. | After cardiac arrest, through study completion (a maximum of 1 year) | |
Secondary | Inter-observer variability in determining the quality of the doppler ultrasound signal. | The sonographer on site will assess the quality of the acquired doppler ultrasound images, as well as two ultrasound experts who will be blinded to the performing sonographer. The difference between these assessments will be analyzed. | After cardiac arrest, through study completion (a maximum of 1 year) |
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