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.
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
- Conditions the study is for
- Out of Hospital Cardiac Arrest, Ventricular Fibrillation, Defibrillation
- 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.
14 sites in 3 countries
Sweden9 sites, 9 recruiting
- 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.
Spain4 sites, 4 recruiting
- Not yet 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.
Netherlands1 site, 1 recruiting
- Not yet 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.
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.
- Conditions
- Out of Hospital Cardiac Arrest, Ventricular Fibrillation, Defibrillation, CPR, ACLS, Sudden Death
- 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 group | Role | What they receive |
|---|---|---|
| Early Double sequential defibrillation | Experimental | 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. Receives: Device: Double sequential defibirllation |
| Standard defibrillation | Active comparator | 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. Receives: Device: Standard defibrillation |
What is being measured
The primary outcome is the main question the study is designed to answer.
30 day survival
Survival at 30 days
Measured: 30 days
Secondary outcomes (4)
ROSC
Any prehospital ROSC, defined as confirmed ROSC by EMS personnel, in accordance with latest Utstein definition
Measured: 1 day
Survival to hospital Admission
Admitted alive to a hospital ward with spontaneous circulation
Measured: 1 day
Survival to hospital discharge
Discharged alive from hospital
Measured: 30 days
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.
- First posted16 Sep 2025
- Study start8 Sep 2025
- Primary completion31 Dec 2028 (estimated)
- Study completionDec 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Out of Hospital Cardiac ArrestStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Gabriel Riva
- Sponsor type
- University, hospital or other
- Collaborators
- Swedish Heart Lung Foundation, Region Stockholm, Vastra Gotaland Region, Region Halland, Laerdal Foundation
- Responsible party
- Sponsor-investigator, Gabriel Riva, Karolinska Institutet
- Investigators
- Gabriel Riva, M.D. Ph.D., Study director, Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, SwedenAkil Awad, M.D. Ph.D., Principal investigator, Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, SwedenCarl Magnusson, R.N., Ph.D., Study chair, Shalgrenska University HospitalAndreas Claesson, R.N. Ph.D., Study chair, Center for resuscitation Science. Department of clinical sience and education. Södersjukhuset, Karolinksa Institutet, Stockholm, SwedenJohan Israelsson, R.N. Ph.D., Study chair, ICARE, Department of Health and Caring Sciences, Linnaeus University
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
Study at a glance
From the registry record, last updated by the sponsor on 17 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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"
- ClinicalTrials.gov ID
- NCT07174986
- Acronym / sponsor ID
- DOUBLE D / CIV-ID-25-01-051015
- Conditions
- Out of Hospital Cardiac Arrest, Ventricular Fibrillation, Defibrillation, CPR, ACLS, Sudden Death
- Keywords
- Double sequential defibrillation, Double sequential external defibrillation, ACLS
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 916 participants (estimated)
- Lead sponsor
- Gabriel RivaUniversity, hospital or other
- Collaborators
- Swedish Heart Lung Foundation, Region Stockholm, Vastra Gotaland Region, Region Halland, Laerdal Foundation
- Study start
- 8 Sep 2025 (actual)
- Primary completion
- 31 Dec 2028 (estimated)
- Study completion
- Dec 2029 (estimated)
- First posted
- 16 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
- Model description
- Academic, investigator initiated, open-label pilot study with a randomized controlled trial (RCT) design
| Arm | Type | Receives |
|---|---|---|
| Early Double sequential defibrillation | Experimental | Device: Double sequential defibirllationIf 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. |
| Standard defibrillation | Active comparator | Device: Standard defibrillationIf 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. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- OHCA patients with VT/VF at first rhythm analysis and at least one defibrillation performed in standard (A-L) position
Key exclusion criteria (3 listed)
- Age < 18 years
- Obvious pregnancy
- Known preexisting Do Not Attempt Resuscitation order
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Double sequential defibirllationAlso: DSDA 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 | Early Double sequential defibrillation |
| Standard defibrillationStandard defibrillation uning one defibrillator | Device | Standard defibrillation |
Primary outcome
30 day survival
Time frame: 30 days
Survival at 30 days
4 secondary outcomes
ROSC
Time frame: 1 day
Survival to hospital Admission
Time frame: 1 day
Survival to hospital discharge
Time frame: 30 days
Neurological function at hospital discharge, mRS (modified Ranking scale, 1-6 where 1 indicates better function)
Time frame: 30 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Feb 2026.
- Derived from this study: PubMed 42379878Riva 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
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
14 sites in 3 countries: see every site and its status.
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.