Early Double Sequential Defibrillation in Out of Hospital Cardiac Arrest

NCT07174986 · Status: RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 916

Last updated 2026-02-17

No results posted yet for this study

Summary

Some of the patients affected by Out-of-hospital cardiac arrest (OHCA) with ventricular fibrillation (VF)/ventricular tachycardia (VT) do not respond to initial defibrillation. The survival decreases with number of defibrillations required to terminate VF/VT. In 2022, one prospective cluster randomized trial showed increased survival among (OHCA) patients in refractory VF using Double Sequential Defibrillation (DSD). If DSD can increase survival among all patients in VF that dont respond to one defibrillation, i.e. before it has become refractory is not known.

The aim of this trial is to assess survival with a double defibrillation strategy initiated as soon as possible among patients with Out of Hospital Cardiac Arrest with initial shockable rhythm and at least one failed standard defibrillation, compared with continued resuscitation using standard defibrillation.

Conditions

  • Out of Hospital Cardiac Arrest
  • Ventricular Fibrillation
  • Defibrillation
  • CPR
  • ACLS
  • Sudden Death

Interventions

DEVICE

Double sequential defibirllation

A second defibrillator will be applyed with electrodes placed in the A-P position and defibrillation will be performed with two defibrllators in a sequential manner

DEVICE

Standard defibrillation

Standard defibrillation uning one defibrillator

Sponsors & Collaborators

  • Swedish Heart Lung Foundation

    collaborator OTHER
  • Region Stockholm

    collaborator OTHER_GOV
  • Vastra Gotaland Region

    collaborator OTHER_GOV
  • Region Halland

    collaborator OTHER
  • Laerdal Foundation

    collaborator OTHER
  • Gabriel Riva

    lead OTHER

Principal Investigators

  • Gabriel Riva, M.D. Ph.D. · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden

  • Akil Awad, M.D. Ph.D. · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden

  • Carl Magnusson, R.N., Ph.D. · Shalgrenska University Hospital

  • Andreas Claesson, R.N. Ph.D. · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden

  • Johan Israelsson, R.N. Ph.D. · ICARE, Department of Health and Caring Sciences, Linnaeus University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-08
Primary Completion
2028-12-31
Completion
2029-12-31

Countries

  • Netherlands
  • Spain
  • 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 NCT07174986 on ClinicalTrials.gov