RescueDoppler- a Disruptive Ultrasound Solution for Improved Outcome After Cardiac Arrest.

NCT06599073 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 285

Last updated 2026-02-27

No results posted yet for this study

Summary

RescueDoppler is an innovative, hands-free Doppler system designed for continuous monitoring of blood flow in the carotid artery, distinguishing between the presence and absence of a pulse. It is non-invasive, user-independent, and does not require specialized ultrasound expertise. The primary goal of this study is to assess the feasibility and clinical utility of RescueDoppler for monitoring carotid artery blood flow in patients experiencing sudden cardiac arrest.

The multi-center study will be performed both pre-hospital and in-hospital.

Conditions

  • Cardiac Arrest (CA)
  • Cardiopulmonary Resuscitation
  • Doppler Ultrasound

Interventions

DEVICE

RescueDoppler

Continuous hands-free Doppler ultrasound of the carotid artery during cardiac arrest

DEVICE

Rescue

RescueDoppler patch with probe is attached on the left side of the neck during the cardiac arrest. Operative health personell are blinded for the velocity curves that are post-processed by the research team after the cardiac arrest and synchronised with ECG.

Sponsors & Collaborators

  • St. Olavs Hospital

    collaborator OTHER
  • Nordlandssykehuset HF

    collaborator OTHER
  • Ullevaal University Hospital

    collaborator OTHER
  • Rikshospitalet University Hospital

    collaborator OTHER
  • University Hospital, Akershus

    collaborator OTHER
  • Haukeland University Hospital

    collaborator OTHER
  • Norwegian University of Science and Technology

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-19
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Norway
  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06599073 on ClinicalTrials.gov