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Early Amiodarone in Shockable Cardiac Arrest
Early Amiodarone in Shockable Cardiac Arrest (Early-Amio) Study
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Emergency medical services (EMS)-treated non-traumatic out-of-hospital cardiac arrest * Initial rhythm on EMS rhythm assessment of ventricular fibrillation or ventricular tachycardia * Recurrence or persistence of ventricular fibrillation or ventricular tachycardia after one defibrillation attempt Exclusion Criteria: * Known allergy to amiodarone * EMS-assessed contraindication to amiodarone * Pre-existing "do-not-attempt-resuscitation" orders * Inter-facility transportations * Initial care by a non-participating EMS agency able to perform advanced life support interventions * Pediatric patient as determined by EMS * Prisoners * Pregnant patients
About the study
The primary objective of this pilot, pragmatic stepped-wedge cluster randomized trial is to evaluate if a modified cardiac arrest treatment algorithm calling for the administration of the initial amiodarone dose one 2-minute cycle earlier than current guidelines (during the same cycle as the initial dose of epinephrine) improves the time to amiodarone delivery in those with out-of-hospital cardiac arrest due to refractory ventricular fibrillation or ventricular tachycardia compared to usual care.
What is being tested
- Amiodarone Hydrochloride Injection (drug)
- Usual Care Protocol (other)
Sponsor: Oregon Health and Science University · Participants: 585 · Started: Jan 1, 2025
Contact the study team
- Joshua Lupton, MD, MPH · Phone: (503) 418-6706
Official record on ClinicalTrials.gov — NCT06680869
Locations in the U.S.
| Oregon | Oregon Health & Sciences University, Portland |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.