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RecruitingNCT07174986DOUBLE DUpdated Feb 17, 2026

Early Double Sequential Defibrillation in Out of Hospital Cardiac Arrest

A Phase 2/3 interventional study of Double sequential defibirllation and Standard defibrillation in Out of Hospital Cardiac Arrest, Ventricular Fibrillation and Defibrillation, sponsored by Gabriel Riva. Recruiting at 14 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-17.

Sponsored by Gabriel Riva · Phase 2/3, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2025; still recruiting 1 year 2 months later.
Phase
Phase 2/3
Study type
Interventional
Enrollment
916
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

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.

Read the detailed description

Background: Out-of-hospital cardiac arrest (OHCA) affects about 270,000 individuals in Europe annually.[1] In OHCA, presenting with ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT) amendable to defibrillation are among the strongest predictors of survival.[2] If defibrillation can be done successfully within the first 3-5 minutes survival can be as high as 70 %.[3] However, some patients in VT/VF do not respond to initial defibrillation, and survival decreases with number of defibrillations required to terminate VT/VF.[4]

In 2022, one prospective cluster randomized trial showed increased survival among OHCA patients in refractory VF using an alternative defibrillation strategy with either, switching to Anterior-Posterior defibrillation pad placements (A-P) or Double Sequential Defibrillation "DSD", (Using two defibrillators, one in the standard anterior-lateral position (A-L) and one in A-P position and defibrillation in rapid sequence) compared to standard defibrillation pad placement.[5] Refractory VF was defined as VF that persisted despite three consecutive defibrillations with defibrillation pads in the standard position.

These results prompted the International Liaison Committee on Resuscitation (ILCOR) to release a statement of treatment recommendation on DSD in March 6, 2023. It suggested that "…either vector change or DSD may be considered for adults with cardiac arrest who remain in VF or pulseless VT despite three defibrillations (weak recommendation, low certainty of evidence)." [6] Further, if DSD would be used it should be performed with a methodology similar to that described in the trial by Cheskes et al.

However, several questions remain. Knowledge gaps highlighted in the ILCOR statement included if the results from this one cluster randomized trial could be reproduced in any other setting. Further, since survival is inversely associated with the number of defibrillation shocks, if earlier application of DSD could lead to even higher survival for patients not in refractory VF has never been studied.

Study rationale: In order to evaluate if an early DSD-strategy could benefit all patients with VT/VF after the first shock, including those not in refractory VF, the Double-D trial is designed. If DSD would prove to be superior to standard defibrillation in a broader cardiac arrest population, also among those not in refractory VF, this would have a large impact on how Advanced Cardiac Life Support (ACLS) should be performed.

Design: This is an academic, investigator initiated, open-label pilot study with a randomized controlled trial (RCT) design and 1:1 allocation (1 DSD: 1 standard). Screening for inclusion will be performed in all cardiac arrests by participating EMS units where there are two study-specific defibrillators available on site.

Study population: Adult OHCA patients with pulseless VT/VF at initial rhythm analysis, at least one defibrillation performed in standard A-L position without return of spontaneous circulation (ROSC).

P: Adult patients, 18 years or older, with OHCA, initial shockable rhythm (VT/VF) and, at least, one defibrillation performed in standard position and ongoing CPR (no ROSC).

I: Application of a second defibrillator with pad-placement in the anterior-posterior (A-P) position as early as possible after the first shock and double sequential defibrillation after the following rhythm analysis if the patient is still in VT/VF.

C: Standard defibrillation electrode placement (A-L) and routine defibrillation with one defibrillator after the following rhythm analysis if the patient is still in VT/VF.

O: Primary outcome is 30-day survival.

The trial will be conducted by participating ambulance units attending OHCA´s. These units will perform screening for inclusion, randomization, intervention or control treatment and initial follow up.

02

Conditions studied

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

Keywords

  • Double sequential defibrillation
  • Double sequential external defibrillation
  • ACLS
03

In context

Out-of-Hospital Cardiac Arrest

314 studies on the registry are indexed under Out-of-Hospital Cardiac Arrest; 93 are open to participants now.

This study's planned enrollment of 916 is above the median of 218 across 179 interventional studies indexed under Out-of-Hospital Cardiac Arrest.

Browse Out-of-Hospital Cardiac Arrest studies →

Lead sponsor

This is the only study on the registry with Gabriel Riva as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • OHCA patients with VT/VF at first rhythm analysis and at least one defibrillation performed in standard (A-L) position

Exclusion criteria

Exclusion Criteria:

  • Age \< 18 years
  • Obvious pregnancy
  • Known preexisting Do Not Attempt Resuscitation order
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
916 participants (estimated)

Study arms

  • Experimental
    Early Double sequential defibrillation

    If the patient is randomized to the DSD group, the ambulance crew team will apply the second defibrillator with electrodes placed in the A-P position as soon as possible. Defibrillation is performed by one person defibrillating both defibrillators in a sequential manner "Double Sequential Defibrillation" (DSD). All consecutive defibrillations will thereafter be performed with the DSD strategy until ROSC, termination of resuscitation or decision to move the patient to hospital.

    Device: Double sequential defibirllation

  • Active comparator
    Standard defibrillation

    If the patient is randomized to the standard defibrillation group, the ambulance crew team will continue Advanced life support in accordance with standard of care and continue to perform standard defibibrillation using one defibrillator. All consecutive defibrillations will thereafter be performed with the standard defibrillation strategy until ROSC, termination of resuscitation or decision to move the patient to hospital.

    Device: Standard defibrillation

Interventions

  • DeviceDouble 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

    Also known as: DSD

  • DeviceStandard defibrillation

    Standard defibrillation uning one defibrillator

06

What researchers measure

Primary outcomes

  1. 30 day survival

    Survival at 30 days

    Time frame: 30 days

Secondary outcomes

  1. ROSC

    Any prehospital ROSC, defined as confirmed ROSC by EMS personnel, in accordance with latest Utstein definition

    Time frame: 1 day

  2. Survival to hospital Admission

    Admitted alive to a hospital ward with spontaneous circulation

    Time frame: 1 day

  3. Survival to hospital discharge

    Discharged alive from hospital

    Time frame: 30 days

  4. Neurological function at hospital discharge, mRS (modified Ranking scale, 1-6 where 1 indicates better function)

    Neurological function at hospital discharge (mRS)

    Time frame: 30 days

Other outcomes

  1. 90 days survival

    Survival to 90 days

    Time frame: 90 days

  2. Neurological function at 90 days (mRS)

    Neurological function at 90 days (modified Ranking scale)

    Time frame: 90 days

  3. Helath related quality of life at 90 days

    Helath related quality of life at 90 days

    Time frame: 90 days

  4. Neurological function at 180 days (mRS)

    Neurological function (modified Ranking Scale)

    Time frame: 180 days

  5. Health related quality of life at 180 days

    Health related quality of life at 180 days

    Time frame: 180 days

  6. Number of defibrillations to sustained ROSC

    Total number of defibrillations to sustained ROSC

    Time frame: 1 day

  7. Termination of ventricular fibrillation

    defined as the presence as a non-shockable rhythm 5 seconds after defibrillation

    Time frame: 1 day

07

Study locations

9 of 14 sites recruiting
  • ARREST (AmsteRdam REsuscitation STudies)
    Amsterdam, Netherlands
    Not yet recruiting
    • Christian Van der Werf, M.D. Ph.D. · Contactc.vanderwerf@amsterdamumc.nl · (+31) 614 42 58 04
    • Christian Van der Werf, M.D. Ph.D. · Principal investigator
  • Centro de Emergencias 061 Andalucía
    Málaga, Andalusia 29560, Spain
    Not yet recruiting
  • Médico Emergencias Osakidetza EMERGENTZIAK
    Bilbao, Baque Country 48004, Spain
    Not yet recruiting
  • Sistema de Emergencias Medicas de Catalunya
    Barcelona, Catalonia 08908, Spain
    Not yet recruiting
  • SUMMA 112 Emergency medical services
    Madrid, Madrid 28045, Spain
    Not yet recruiting
  • Ambulanssjukvården, Region Halland
    Halmstad, Halland County, Sweden
    Recruiting
  • Ambulanssjukvården Region Värmland
    Karlstad, Värmland County 65230, Sweden
    Recruiting
  • Ambulanshelikoptern (HEMS) Västra Götalandsregionen
    Kungälv, Västra Götaland County 442 83, Sweden
    Recruiting
    • Knut Taxbro, M.D. Ph.D. · Contactknut.taxbro@rjl.se · (+46) 070 675 34 57
    • Knut Taxbro, M.D. Ph.D. · Principal investigator
  • Sjukvården i väster
    Alingsås, Sweden
    Recruiting
    • Andreas Claesson, R.N. Ph.D. · ContactAndreas.claesson@ki.se · (+46) 0704940546
    • Andreas Claesson, R.N. Ph.D. · Principal investigator
  • Emergency medical services, Södra Älvsborgs Sjukhus, Region Västra Götaland
    Borås, 501 82, Sweden
    Recruiting
    • Emil Bergerum, R.N. · Contactemil.j.olsson@vgregion.se · 0046 (0)33 - 616 10 00
    • Emil Bergerum, R.N. · Principal investigator
  • Prehospital Intensive Care Unit (PIV) AnOPIVA Östra Sjukhuset/SU
    Gothenburg, Sweden
    Recruiting
    • Patrik Martner, M.D. · Contactpatrik.martner@vgregion.se · (+46) 070 485 77 52
    • Patrik Martner, M.D. · Principal investigator
  • Shalgrenska University Hospital
    Gothenburg, Sweden
    Recruiting
  • Ambulanssjukvården Skaraborgs Sjukhus, Västra Götalandsregionen (SKAS)
    Skövde, Sweden
    Recruiting
    • Per Wennberg, R.N. Ph.D. · Contactper.wennberg@vgregion.se · 0046 70 545 20 86
    • Per Wennberg, R.N. Ph.D. · Principal investigator
  • Emergency medical services NU-Sjukvården, Region Västra Götaland
    Trollhättan, 461 85, Sweden
    Recruiting
    • Carl Magnusson, R.N. Ph.D. · Contactcarl.magnusson@vgregion.se · 0046 (0)10-435 10 35
    • Carl Magnusson, R.N. Ph.D. · Principal investigator
08

References and documents

Publications

  • Riva G, Nordkvist EB, Magnusson C, Claesson A, Jonsson M, Israelsson J, Nordius C, Barret K, Sidebottom DB, Martner P, Cavefors O, Tenning A, Wibring K, Waldemar A, Edholm G, Awad A. Feasibility of early double sequential defibrillation in out-of-hospital cardiac arrest: the double-D randomised pilot trial. Heart. 2026 Jun 30:heartjnl-2026-327905. doi: 10.1136/heartjnl-2026-327905. Online ahead of print. PubMed 42379878 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2025 (actual). Primary completion is estimated for Dec 2028, 39 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 3, 2025
First posted
Sep 16, 2025
StartActual
Sep 8, 2025
Primary completionEst.
Dec 31, 2028
CompletionEst.
Dec 2029
Last update
Feb 17, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07174986
Lead sponsor
Gabriel Riva
Collaborators
Swedish Heart Lung Foundation, Region Stockholm, Vastra Gotaland Region, Region Halland, Laerdal Foundation
Responsible party
Gabriel Riva (Principal Investigator, Karolinska Institutet) — Sponsor-investigator
First posted
Sep 16, 2025
Start date
Sep 8, 2025
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 2029 (estimated)
Last update
Feb 17, 2026

Study contacts

Gabriel Riva, M.D. Ph.D
Contact
gabriel.riva@ki.se
+ 47 70 545 20 86
Akil Awad, M.D. Ph.D.
Contact
akil.awad@ki.se
(+46) 070 400 13 63
Gabriel Riva, M.D. Ph.D.
study director · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden
Akil Awad, M.D. Ph.D.
principal investigator · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden
Carl Magnusson, R.N., Ph.D.
study chair · Shalgrenska University Hospital
Andreas Claesson, R.N. Ph.D.
study chair · Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, Sweden
Johan Israelsson, R.N. Ph.D.
study chair · ICARE, Department of Health and Caring Sciences, Linnaeus University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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