Last updated: December 19, 2024
Sponsor: Christian Hassager
Overall Status: Active - Recruiting
Phase
2
Condition
N/ATreatment
propofol
esketamine hydrochloride
Clinical Study ID
NCT06744361
2024-515987-29-00
2024-515987-29-00
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults (age ≥18 years) AND
resuscitated OHCA of presumed cardiac cause with a shockable first recorded heartrhythm AND
mean arterial pressure (MAP) >40 mmHg AND
a decision to perform prehospital intubation.
Exclusion
Exclusion Criteria:
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.
Study Design
Total Participants: 282
Treatment Group(s): 2
Primary Treatment: propofol
Phase: 2
Study Start date:
December 12, 2024
Estimated Completion Date:
September 01, 2027
Connect with a study center
Department of Cardiology, Rigshospitalet
Copenhagen, 2100
DenmarkActive - Recruiting
Odense University Hospital
Odense C, 5000
DenmarkSite Not Available
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