RecruitingPhase 2NCT06744361

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

KETamine Sedation As Neuroprotective Agent Following Out-of-hospital Cardiac Arrest (OHCA) - the KETOHCA Trial


Sponsor

Christian Hassager

Enrollment

282 participants

Start Date

Dec 12, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 18 Years

Inclusion Criteria4

  • 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.

Exclusion Criteria5

  • 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
  • Body temperature <30° C.

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Interventions

DRUGesketamine hydrochloride

Prehospital intravenous or intraosseous bolus administration at a minimum of 0.5 mg/kg of esketamine

DRUGpropofol

Prehospital intravenous or intraosseous bolus administration at a minimum dose of 0.25 mg/kg propofol


Locations(2)

Department of Cardiology, Rigshospitalet

Copenhagen, Denmark

Odense University Hospital

Odense C, Denmark

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NCT06744361


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