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Out of Hospital Cardiac ArrestPhase 2/3DOUBLE DNCT07174986

Early Double Sequential Defibrillation in Out of Hospital Cardiac Arrest

A Phase 2/3 study testing Double sequential defibirllation and Standard defibrillation in people with Out of Hospital Cardiac Arrest and Ventricular Fibrillation, run by Gabriel Riva at 14 sites in 3 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Double sequential defibirllation and Standard defibrillation
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
916 participants
Where
14 sitesin 3 countries
Study dates
8 Sep 2025to Dec 2029
Phase
Phase 2/3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

14 sites in 3 countries. Contact the study team or a site near you to ask about taking part.

Gabriel Riva, M.D. Ph.D contact

+ 47 70 545 20 86

gabriel.riva@ki.se

Akil Awad, M.D. Ph.D. contact

(+46) 070 400 13 63

akil.awad@ki.se

14 sites in 3 countries

Sweden9 sites, 9 recruiting
  • Sjukvården i väster

    Alingsås

    Andreas Claesson, R.N. Ph.D., (+46) 0704940546, Andreas.claesson@ki.se

    Andreas Claesson, R.N. Ph.D.

    Recruiting
  • Emergency medical services, Södra Älvsborgs Sjukhus, Region Västra Götaland

    Borås, 501 82

    Emil Bergerum, R.N., 0046 (0)33 - 616 10 00, emil.j.olsson@vgregion.se

    Emil Bergerum, R.N.

    Recruiting
  • Prehospital Intensive Care Unit (PIV) AnOPIVA Östra Sjukhuset/SU

    Gothenburg

    Patrik Martner, M.D., (+46) 070 485 77 52, patrik.martner@vgregion.se

    Patrik Martner, M.D.

    Recruiting
  • Shalgrenska University Hospital

    Gothenburg

    Carl Magnusson, R.N. Ph.D., carl.magnusson@vgregion.se

    Carl Magnusson, R.N. Ph.D.

    Recruiting
  • Ambulanssjukvården, Region Halland

    Halmstad, Halland County

    Kristoffer Wibring, R.N., Ph.D., (+46) 076 721 40, kristoffer.wibring@regionhalland.se

    Kristoffer Wibring, R.N. Ph.D.

    Recruiting
  • Ambulanssjukvården Region Värmland

    Karlstad, Värmland County, 65230

    Linus Lilja, M.D. Ph.D., (46+) 010-83 157 16, linus.lilja@regionvarmland.se

    Linus Lilja, M.D. Ph.D.

    Recruiting
  • Ambulanshelikoptern (HEMS) Västra Götalandsregionen

    Kungälv, Västra Götaland County, 442 83

    Knut Taxbro, M.D. Ph.D., (+46) 070 675 34 57, knut.taxbro@rjl.se

    Knut Taxbro, M.D. Ph.D.

    Recruiting
  • Ambulanssjukvården Skaraborgs Sjukhus, Västra Götalandsregionen (SKAS)

    Skövde

    Per Wennberg, R.N. Ph.D., 0046 70 545 20 86, per.wennberg@vgregion.se

    Per Wennberg, R.N. Ph.D.

    Recruiting
  • Emergency medical services NU-Sjukvården, Region Västra Götaland

    Trollhättan, 461 85

    Carl Magnusson, R.N. Ph.D., 0046 (0)10-435 10 35, carl.magnusson@vgregion.se

    Carl Magnusson, R.N. Ph.D.

    Recruiting

Other trials in Sweden

Spain4 sites, 4 recruiting
  • Sistema de Emergencias Medicas de Catalunya

    Barcelona, Catalonia, 08908

    Xavier Fabrega, M.D. Ph.D., (+34) 616 44 60 68, francescxavierjimenez@gencat.cat

    Xavier Fabrega, M.D. Ph.D.

    Not yet recruiting
  • Médico Emergencias Osakidetza EMERGENTZIAK

    Bilbao, Baque Country, 48004

    Cristian Fernández Barreras, M.D., (+34) 99 68 11 82, cristian.fernandezbarreras@osakidetza.eus

    Cristian Barreras, M.D.

    Not yet recruiting
  • SUMMA 112 Emergency medical services

    Madrid, Madrid, 28045

    Carlos Rubio, M.D. Ph.D., (+34) 639 91 74 03, carlos.rubio@salud.madrid.org

    Carlos Rubio, M.D. Ph.D.

    Not yet recruiting
  • Centro de Emergencias 061 Andalucía

    Málaga, Andalusia, 29560

    María Jose Luque-Hernández, M.D. Ph.D., (+34) 617 56 33 52, mariajose.luque.sspa@juntadeandalucia.es

    Maria Jose Luque-Hernández, M.D. Ph.D.

    Not yet recruiting

Other trials in Spain

Netherlands1 site, 1 recruiting
  • ARREST (AmsteRdam REsuscitation STudies)

    Amsterdam

    Christian Van der Werf, M.D. Ph.D., (+31) 614 42 58 04, c.vanderwerf@amsterdamumc.nl

    Christian Van der Werf, M.D. Ph.D.

    Not yet recruiting

Other trials in Netherlands

About this study

Official title: "A Randomized Trial Assessing the Effect of Early Double Sequential Defibrillation With Anterior-posterior and Anterior Lateral Pad Placement and Sequential Defibrillation Compared to Standard Pad Placement and Single Defibrillation in Patients With Out of Hospital Cardiac Arrest With Initial Shockable Rhythm and at Least One Failed Standard Defibrillation"

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.

Being tested
Double sequential defibirllation, Standard defibrillation
Keywords
Double sequential defibrillation, Double sequential external defibrillation, ACLS
Medical subject headings
Out-of-Hospital Cardiac Arrest, Ventricular Fibrillation, Death, Sudden

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Double sequential defibirllationDevice

    Also called DSD

    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

  • Standard defibrillationDevice

    Standard defibrillation uning one defibrillator

Study groups in NCT07174986
Study groupRoleWhat they receive
Early Double sequential defibrillationExperimentalIf 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.
Receives: Device: Double sequential defibirllation
Standard defibrillationActive comparatorIf 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.
Receives: Device: Standard defibrillation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 30 day survival

    Survival at 30 days

    Measured: 30 days

Secondary outcomes (4)
  1. ROSC

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

    Measured: 1 day

  2. Survival to hospital Admission

    Admitted alive to a hospital ward with spontaneous circulation

    Measured: 1 day

  3. Survival to hospital discharge

    Discharged alive from hospital

    Measured: 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)

    Measured: 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2025
  2. Study start8 Sep 2025
  3. Primary completion31 Dec 2028 (estimated)
  4. Study completionDec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Academic, investigator initiated, open-label pilot study with a randomized controlled trial (RCT) design
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
916 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07174986
Sponsor's protocol ID
CIV-ID-25-01-051015
Other IDs
Dnr 2025-03532-01
Acronym
DOUBLE D
Status last verified
Feb 2026
First submitted
3 Sep 2025
Last updated
17 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

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

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing Double sequential defibirllation and Standard defibrillation in people with Out of Hospital Cardiac Arrest and Ventricular Fibrillation, run by Gabriel Riva at 14 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 14 sites in Sweden, Spain, Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Gabriel Riva, M.D. Ph.D (+ 47 70 545 20 86, gabriel.riva@ki.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

30 day survival (time frame: 30 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07174986, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Feb 2026.

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