The Application of Ketamine for Sedation in Patients With Cardiac Arrest - - KetCat (KETamine in Cardiac ArresT) Study
NCT ID: NCT04360070
Last Updated: 2023-01-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
24 participants
INTERVENTIONAL
2022-02-28
2023-12-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Ketamine Arm
Patients randomized to the ketamine arm will receive ketamine as part of their sedation medications during their cardiac arrest treatment
Ketamine Hydrochloride
Parenteral General Anesthetic
Control Arm
Patients randomized to the control arm will not receive ketamine as part of their sedation medications during their cardiac arrest treatment.
No interventions assigned to this group
Interventions
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Ketamine Hydrochloride
Parenteral General Anesthetic
Eligibility Criteria
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Inclusion Criteria
* Over 19 years of age
* Patients requiring sedation based on the assessment of the resuscitating physician.
Exclusion Criteria
* Any history of previous, pre-existing neurological deficit
* Started on Extracorporeal Membrane Oxygenation (ECMO)
* Duration of cardiac arrest without ROSC is greater than 30 consecutive minutes
* Known contraindication or hypersensitivity to ketamine
* Awake patient or no standard sedation or no intubation required
* Inability to obtain deferred consent
* Currently enrolled in any other research study involving drugs or devices
* Patients who are pregnant
* Patients who are prisoners
* Patients residing in Long Term Care (LTC) facilities
19 Years
ALL
No
Sponsors
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Fraser Health
OTHER
Responsible Party
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George Medvedev
Head of Neurology
Locations
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Fraser Health Authority - Royal Columbian Hospital
New Westminster, British Columbia, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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001
Identifier Type: -
Identifier Source: org_study_id
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