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Effects of Epinephrine and Intravenous (I.V.) Needle on Cardiopulmonary Resuscitation (CPR) Outcome

Phase 2
Completed
Conditions
Cardiac Arrest
Interventions
Registration Number
NCT00121524
Lead Sponsor
Petter Andreas Steen
Brief Summary

Intravenous epinephrine has been part of the guidelines for cardiopulmonary resuscitation since the start. It improves outcome in animal studies, but has never been investigated in a controlled study in humans. Epidemiologic data indicate that it is an independent negative predictor for survival. If this is true in a controlled randomized study, it could be due to effects of the drug itself or more likely due to reduced quality of chest compressions and ventilations due to the time spent on placing an I.V. needle and injecting drugs.

Detailed Description

In a randomized, controlled study of all out-of-hospital cardiac arrest patients in Oslo, Norway, half the patients are treated according to the international guidelines for advanced CPR, and the other half according to the same guidelines, except for no I.V. needle or drugs are given until 5 minutes after eventual return of spontaneous circulation.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
904
Inclusion Criteria
  • Cardiac arrest out-of-hospital
Exclusion Criteria
  • <18 years old
  • Trauma as cause of arrest

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
IV yesEpinephrineIntravenous needle Epinephrine q 3 min during CPR Atropine 3 mg in initial asystole Amiodarone 300 mg iv after repeated failed defibrillation attempts
IV yesIntravenous needleIntravenous needle Epinephrine q 3 min during CPR Atropine 3 mg in initial asystole Amiodarone 300 mg iv after repeated failed defibrillation attempts
IV yesAtropineIntravenous needle Epinephrine q 3 min during CPR Atropine 3 mg in initial asystole Amiodarone 300 mg iv after repeated failed defibrillation attempts
IV yesAmiodaroneIntravenous needle Epinephrine q 3 min during CPR Atropine 3 mg in initial asystole Amiodarone 300 mg iv after repeated failed defibrillation attempts
Primary Outcome Measures
NameTimeMethod
survival to hospital discharge with neurologic outcomedischarge from hospital
Secondary Outcome Measures
NameTimeMethod
admit to hospital with spontaneous circulationhospital admission
one year survival with neurologic outcomeone year after hospital discharge

Trial Locations

Locations (1)

Ulleval University Hospital

🇳🇴

Oslo, Norway

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