NCT06491186

Brief Summary

The goal of this prospective observational study is to investigate B-mode point-of care ultrasound with arterial compressibility assessment on the femoral artery as a method to determine the presence of a pulse and to compare it with concurrently conducted manual pulse checks.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
69

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 1, 2024

Completed
1 day until next milestone

Study Start

First participant enrolled

May 2, 2024

Completed
2 months until next milestone

First Posted

Study publicly available on registry

July 9, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

July 9, 2024

Status Verified

June 1, 2024

Enrollment Period

8 months

First QC Date

May 1, 2024

Last Update Submit

June 29, 2024

Conditions

Keywords

Cardiac ArrestOut-of-hospital Cardiac ArrestOHCAUltrasoundPoint-Of-Care UltrasoundPOCUSPulse CheckPOCUS Pulse CheckB-mode UltrasoundFemoral ArteryArterial Compressibility Assessment

Outcome Measures

Primary Outcomes (2)

  • Results of POCUS pulse check

    If the femoral artery is both non-compressible and pulsatile, the POCUS pulse check will be considered positive

    During cardiac arrest, up to 45 minutes

  • Results of the concurrently conducted manual pulse check

    Parallel to our study team the treating team will conduct standard care, consisting of determining the presence or absence of a pulse by palpation. The results of these manual pulse checks will be recorded by our study team.

    During cardiac arrest, up to 45 minutes

Secondary Outcomes (4)

  • Arterial compressibility during chest compressions

    During cardiac arrest, up to 45 minutes

  • Arterial compressibility during rhythm checks

    During cardiac arrest, up to 45 minutes

  • Arterial pulsatility during rhythm checks

    During cardiac arrest, up to 45 minutes

  • Time needed for POCUS pulse checks

    During cardiac arrest, up to 45 minutes

Study Arms (1)

Included patients

Other: Point of Care Ultrasound

Interventions

Point-of-care ultrasound will be used to image the femoral vessels and to assess the presence or absence of a pulse and the compressibility of the artery during rhythm checks.

Included patients

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population comprises non-pregnant adults suffering out-of-hospital cardiac arrest of any cause who are treated with CPR by emergency medical services.

You may qualify if:

  • Out-of-hospital cardiac arrest treated by EMS
  • Minimum age of 18 years

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Emergency Medical Service of Vienna

Vienna, 1030, Austria

RECRUITING

MeSH Terms

Conditions

Out-of-Hospital Cardiac ArrestHeart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Philipp Metelka, MD

    Medical University of Vienna

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Christina Hafner, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident

Study Record Dates

First Submitted

May 1, 2024

First Posted

July 9, 2024

Study Start

May 2, 2024

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

July 9, 2024

Record last verified: 2024-06

Locations