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Out-Of-Hospital Cardiac ArrestPhase 4EPISONCT06473116

Epinephrine Versus Isoprenaline During Out-of-Hospital Cardiac Arrest With Asystole

A Phase 4 study testing Isoprenaline Only Product in people with Out-Of-Hospital Cardiac Arrest, run by University of Southern Denmark at 1 site in Denmark.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Background: During out-of-hospital cardiac arrest (OHCA), the patient presents with either a shockable or a non-shockable rhythm. Early cardiopulmonary resuscitation (CPR) and defibrillation of the shockable rhythm may increase chance of survival to more than 50%, however, if untreated, the heart rhythm will… Read more about this study

Who is it for?
Ages 18 to 85 yearsHealthy volunteers can take part
Conditions the study is for
Out-Of-Hospital Cardiac Arrest
What is being tested?
Isoprenaline Only Product
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,178 participants
Where
1 siteDenmark
Study dates
Mar 2025to Jul 2029
Phase
Phase 4
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 to 85 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Witnessed out-of-hospital cardiac arrest
  • Age 18 years or more
  • Initial rhythm asystole at EMS arrival
  • Advanced life support initiated or continued by EMS personnel

Who cannot join

  • Cardiac arrest caused by blunt trauma, penetrating trauma, or burn injury suspected to be the cause of the cardiac arrest
  • Cardiac arrest caused by drowning, hanging, strangulation, and foreign body airway obstruction
  • IV epinephrine already administered prior to EMS arrival
  • Prior enrollment in the trial
  • Known or apparent pregnancy
  • Cardiac arrest at nursing homes

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Denmark1 site
  • Research Department of Cardiology

    Odense, 5000

    Laura Sarkisian, MD, PhD, 27859444, sarkisian86@hotmail.com

Other trials in Denmark

About this study

Official title: Epinephrine Versus Isoprenaline During Out-of-Hospital Cardiac Arrest With Asystole: A Randomized Clinical Trial

Background: During out-of-hospital cardiac arrest (OHCA), the patient presents with either a shockable or a non-shockable rhythm. Early cardiopulmonary resuscitation (CPR) and defibrillation of the shockable rhythm may increase chance of survival to more than 50%, however, if untreated, the heart rhythm will deteriorate to a non-shockable rhythm with dismal survival outcomes of 1-5%. Isoprenaline is a pro-arrhythmic drug used to treat bradycardia, and has a structural resemblance to epinephrine, which is the drug of choice during cardiac arrest with non-shockable rhythms.

Aims: To evaluate whether intravebous (IV) administration of isoprenaline increases the chance of return of spontaneous circulation (ROSC) to hospital arrival (main outcome) compared with IV epinephrine.

Read more

Study design: A randomized-controlled trial.

Setting: The study will be conducted in the Region of Southern Denmark, which has about 1.2 million inhabitants and an annual incidence of 1,200 OHCAs. The study will include bystander-witnessed patients with asystole at the arrival of the emergency medical services (EMS). Randomization will take place on arrival of the EMS, where the OHCA patients randomly will be assigned to receive an intravenous injection of isoprenaline (600 µg) or an intravenous injection of adrenaline (1 mg) in a 1:1 ratio. The study will include 1,178 OHCAs over a time period of about 3.5 years.

Read the detailed description

Background: Out-of-hospital cardiac arrest (OHCA) is the leading cause of death in industrialized countries. During OHCA, the patient will present with either a non-shockable or a shockable rhythm. A shockable rhythm is treated by defibrillation, which means delivering an electrical shock through the heart to reestablish normal cardiac electric activity. If a shockable rhythm is defibrillated early, chances of survival can exceed 50%. However, if the shockable rhythm remains untreated, it will deteriorate into a non-shockable rhythm with dismal survival rates of 1-5%. Epinephrine increases the chance of return of spontaneous circulation (ROSC), however, there is increasing evidence that use of epinephrine is associated with severe neurological impairment in survivors. Isoprenaline is a pro-arrhythmic drug used to treat bradycardia. The drug has structural resemblance to epinephrine, however, it has no effect on alfa-adrenoceptors in the cerebral bloodflow and only stimulates beta-adrenoceptors. These pro-arrhythmic properties may induce cardiac electrical activity during OHCA with a non-shockable rhythm, converting it to a shockable rhythm treatable by defibrillation, while preserving microcirculatory cerebral blood flow.

Hypothesis: Injection of isoprenaline in bystander witnessed OHCAs with asystole increases the chance of ROSC at hospital arrival compared with the injection of epinephrine.

Population: According to the Danish Cardiac Arrest Registry, the annual incidence of OHCAs in the Region of Southern Denmark is about 1200, half of which are bystander witnessed. In the recent 2022 report, the incidence of non-shockable first rhythm among these was 1,044 out of 1,233 patients (85%), of which about 9 out of 10 had asystole. Therefore, an annual number of 450 bystander witnessed OHCAs with non-shockable rhythm could be eligible for study entry, however, despite eligibility, previous study have found that about 20-25% of patients are not enrolled in similar OHCA trials, and the expected annual number of enrollments will therefore be 360 OHCAs.

Settings: The study will take place in the Region of Southern Denmark. The Region has 42 EMS ambulance stations and 6 physician-manned vehicles with a median response time of about 8 minutes. The EMS ambulance has an emergency medical technician (EMT) and an EMT assistant, trained in analysing shockable/non-shockable rhythms and administering intravenous drugs according to the advanced life support algorithm.

Intervention: On EMS arrival, OHCA patients will be randomly assigned to receive an intravenous injection of isoprenaline or to receive an intravenous injection of adrenaline in a 1:1 ratio.

Study design: A randomized-controlled trial.

Main outcome: Main outcome is ROSC at hospital arrival. Secondary outcomes are conversion from non-shockable to shockable rhythm, 30-day survival with good neurological outcome (Cerebral Performance Category Scale of 1 or 2).

Power analysis: Thirty-day survival among OHCAs with non-shockable rhythm is reported at 1-5%. In a Danish study, the conversion of a non-shockable rhythm to a shockable rhythm increased the rate of ROSC at hospital arrival to 14.5% compared with 8.4% for sustained non-shockable rhythms. Thirty-day survival in the two groups were 4.2% versus 1.2%, respectively. According to this study, about 1 in 8 non-shockable rhythms converted to a shockable rhythm. Presuming that isoprenaline injection may double the conversion to shockable rhythm to 1 in 4 non-shockable rhythms, this would increased chance of ROSC at hospital arrival to approximately 13%. Therefore, assuming a conservative difference estimate of about 5% (estimate of 13% in the intervention group and 8% in the control group), this study will require a total sample size of 1178 patients with 589 OHCAs in each group (power value of 0.80 and significance level of 0.05) to evaluate the hypothesis. An inclusion time of approximately 3.5 years is therefore to be expected.

Being tested
Isoprenaline Only Product
Medical subject headings
Out-of-Hospital Cardiac Arrest

What participants receive

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

  • Isoprenaline Only ProductDrug

    Also called isoproterenol

    Administration of intravenous isoprenaline of 600 mikrograms immediately after recognition of asystole in bystander-witnessed out-of-hospital cardiac arrest

Study groups in NCT06473116
Study groupRoleWhat they receive
Intervention groupExperimentalIsoprenaline
Receives: Drug: Isoprenaline Only Product
Control groupActive comparatorEpinephrine (adrenaline)
Receives: Drug: Isoprenaline Only Product

What is being measured

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

  1. Rate of Return of Spontaneous Circulation (ROSC) at hospital arrival

    Arrival to hospital admission

    Measured: Up to 2 hours

Secondary outcomes (4)
  1. Rate of conversions from asystole to shockable rhythm

    The conversion from asystole to either pulseless ventricular tachycardia or ventricular fibrillation during cardiac arrest resuscitation

    Measured: Up to 1 hour

  2. Number of participants with favorable neurological outcome at hospital discharge

    The modified Rankin Scale (mRS) is ranked from 0 to 6 and defined the following way: A score of 0) represents no symptoms; 1) no significant disability; 2) slight disability; 3) moderate disability; 4) moderately severe disability; 5) severe disability and 6) death. Favorable neurological outcome is defined as mRS score of 0-3.

    Measured: Median hospital stay is about 24 days after out-of-hospital cardiac arrest

  3. TNumber of participants alive after 30 days

    Survival at 30 days after the out-of-hospital cardiac arrest

    Measured: At 30 days

  4. Number of participants who gain sustained return of spontaneous circulation

    The patient achieved sustained return of spontaneous circulation (ROSC), defined as ROSC of at least 20 minutes after the cardiac arrest. ROSC is defined as the resumption of a sustained heart rhythm that perfuses the body after cardiac arrest.

    Measured: 20-50 minutes

Timeline

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

  1. First posted25 Jun 2024
  2. Study startMar 2025 (estimated)
  3. Primary completionJul 2029 (estimated)
  4. Study completionJul 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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
1,178 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06473116
Sponsor's protocol ID
EPISOTrial
Acronym
EPISO
Status last verified
Jun 2024
First submitted
5 Jun 2024
Last updated
25 Jun 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Six months after the publication of the last results, all de-identified individual patient data will be made available for data sharing, and there will be no predetermined end date for the data sharing. Data will be completely anonymized according to Danish law. The main protocol, data dictionary for the REDCap database and the statistical analyses will also be made available. Interested parties with appropriate approval and methodologically sound proposals will be able to request the trial data by contacting the principal investigator and considered for data sharing.

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Isoprenaline Only Product in people with Out-Of-Hospital Cardiac Arrest, run by University of Southern Denmark at 1 site in Denmark.

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 4 inclusion and 6 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: opening soon, as of the sponsor's last update on 25 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. 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 phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

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?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of Return of Spontaneous Circulation (ROSC) at hospital arrival (time frame: Up to 2 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 25 Jun 2024.

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