Skip to content

Strategies for Defibrillation During Out-of-Hospital Cardiac Arrest

Strategies for Defibrillation During Out-of-Hospital Cardiac Arrest - A Randomized Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06781892
Acronym
STRAT-DEFI
Enrollment
909
Registered
2025-01-17
Start date
2025-03-15
Completion date
2029-03-01
Last updated
2025-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest (CA)

Keywords

Out-of-hospital cardiac arrest, Defibrillation, Double-sequential defibrillation

Brief summary

The Strategies for Defibrillation during Out-of-Hospital Cardiac Arrest (STRAT-DEFI) trial is an investigator-initiated, individually randomized, 3-group clinical trial comparing standard anterior-lateral pad positioning with anterior-posterior positioning and double sequential defibrillation during adult out-of-hospital cardiac arrest.

Interventions

OTHERAnterior-lateral pad positioning

Defibrillation pads positioned anterior-lateral

OTHERAnterior-posterior pad positioning

Defibrillation pads positioned anterior-posterior

Combination of anterior-lateral and anterior-posterior pad positioning for a total of 4 pads and 2 shocks.

Sponsors

University of Aarhus
CollaboratorOTHER
Lars Wiuff Andersen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Out-of-hospital cardiac arrest 2. Age ≥ 18 years 3. ≥ 1 manual defibrillation attempt by emergency medical services 4. Shockable rhythm as the last known rhythm 5. Two manual defibrillators present on-site

Exclusion criteria

1. Blunt trauma, penetrating trauma, or burn injury suspected to be the cause of the cardiac arrest 2. Prior enrollment in the trial 3. Posterior pad placement not deemed possible by on-site clinician

Design outcomes

Primary

MeasureTime frame
Survival at 30 days30 days after the cardiac arrest

Secondary

MeasureTime frameDescription
Survival at 90 days90 days after the cardiac arrest
Favorable neurological outcome at 30 days30 days after the cardiac arrestNeurological outcome will be assessed with the modified Rankin Scale (mRS) which is a scale from 0 to 6 assessing neurological/functional outcomes after brain damage with higher scores indicating worse neurological/functional outcomes. The scale will will be dichotomized as favorable (mRS 0-3) vs. unfavorable (mRS 4-6).
Favorable neurological outcome at 90 days90 days after the cardiac arrestNeurological outcome will be assessed with the modified Rankin Scale (mRS) which is a scale from 0 to 6 assessing neurological/functional outcomes after brain damage with higher scores indicating worse neurological/functional outcomes. The scale will will be dichotomized as favorable (mRS 0-3) vs. unfavorable (mRS 4-6).

Countries

Denmark

Contacts

Primary ContactLars W Andersen
lwandersen@clin.au.dk+4578414848
Backup ContactBertram L Kirkegaard
bertramkirkegaard@clin.au.dk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026