Ketamine Sedation As Neuroprotective Agent Following Out-of-hospital Cardiac Arrest

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorChristian Hassager

About this trial

OHCA is a critical medical emergency with significant mortality and morbidity primarily due to hypoxic-ischemic brain injury (HIBI). Despite advances in resuscitation techniques, the neurological outcomes for survivors remain poor. Current post-resuscitation practices lack specific neuroprotective strategies. Ketamine, an N-Methyl-D-Aspartate (NMDA) receptor antagonist, has shown potential neuroprotective properties in preclinical and clinical studies due to its ability to inhibit excitotoxicity and reduce neuronal apoptosis. This trial hypothesizes that ketamine, when used for sedation in OHCA patients, may offer superior neuroprotective benefits compared to the commonly used sedative propofol. By comparing the effects of ketamine and propofol on neuronal damage markers and long-term neurological outcomes, this study aims to identify a potentially effective intervention to improve the prognosis of OHCA patients.

Eligibility criteria

Qualifiers

Adults (age ≥18 years) AND

resuscitated OHCA of presumed cardiac cause with a shockable first recorded heart rhythm AND

mean arterial pressure (MAP) >40 mmHg AND

a decision to perform prehospital intubation.

Disqualifiers

Advanced life support termination-of-resuscitation (TOR) criteria met

Systolic blood pressure >190 mmHg

Known allergy to ketamine or propofol

Chronic diseases making 180-day survival unlikely

Trial design

Treatments tested in this trial

  • esketamine hydrochloride
  • propofol

Treatment groups

282 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Christian Hassager

Lead sponsor

Rigshospitalet, Denmark

Sponsor institution