Effect of Ketamine and Etomidate During RSI on Long Term Outcomes

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Vanderbilt University Medical Center
Study ID
NCT06179485
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Ketamine — DRUG
    The RSI-LTO study collects long-term outcomes from the RSI trial (NCT05277896). In the RSI trial, patients in the ketamine group will be assigned to receive intravenous ketamine for induction of anesthesia during tracheal intubation. A dose of 2 mg/kg will be recommended, and the group assignment sheet will contain a nomogram providing the recommended dose for a range of patient weights (in pounds and kg). Treating clinicians will be able elect to give a lesser or greater dose of ketamine than recommended if felt to be required for optimal patient care.
  • Etomidate — DRUG
    The RSI-LTO study collects long-term outcomes from the RSI trial (NCT05277896). In the RSI trial, patients in the etomidate group will be assigned to receive intravenous etomidate for induction of anesthesia during tracheal intubation. A dose of 0.3 mg/kg will be recommended, and the group assignment sheet will contain a nomogram providing the recommended dose for a range of patient weights (in pounds and kg). Treating clinicians will be able elect to give a lesser or greater dose of etomidate than recommended if felt to be required for optimal patient care.

Study Details

The RSI-LTO study collects long-term outcomes from the RSI trial (NCT05277896). One-third of adults who are intubated in the ED or ICU experience symptoms of posttraumatic stress disorder (PTSD). PTSD is a psychiatric disorder triggered by a "shocking, scary, or dangerous event." Critical illness, tracheal intubation, and mechanical ventilation can be traumatic and distressing events. Patients may recall the intubation procedure, the feeling of the breathing tube in their throat, or being unable to move ("paralyzed"). While on the breathing machine, patients may experience delirium, frightening hallucinations, and delusions. Patients with PTSD after critical illness can be hypervigilant, anxious, and troubled by intrusive thoughts, nightmares, and flashbacks that last months to years after critical illness and that PTSD negatively impacts patients' marriages, work, and quality of life and increases patients' risk of depression, anxiety, substance use disorder, and suicide. Ketamine may prevent PTSD symptoms by blocking the pathways in the brain's glutaminergic system that are responsible for the formation of traumatic memories In outpatients with chronic PTSD, a single dose of ketamine has been shown to reduce PTSD symptoms for up to 2 weeks. Even a modest reduction in PTSD would translate into tens of thousands of fewer cases of PTSD each year, more cases of PTSD each year than any other medical intervention evaluated to date.

Key Dates

Start date
Apr 6, 2022
Status verified
May 2026
Primary completion
Jan 31, 2027
Completion
Mar 31, 2028

Study Design

Enrollment
1,756 participants (estimated)

Arms

  • Arm: Comparator: Ketamine Group
    Intravenous ketamine as the sedative for induction of anesthesia during emergency tracheal intubation.
  • Arm: Comparator: Etomidate Group
    Intravenous etomidate as the sedative for induction of anesthesia during emergency tracheal intubation.

Primary Outcome Measure

PTSD Symptoms at 12 months [ Time Frame: 12 months ]

Locations (6)

FacilityCityStateZIPSite coordinators
University of Alabama HospitalBirminghamAlabama35233-
University of Colorado DenverAuroraColorado80045-
Denver Health Medical CenterDenverColorado80204-
Hennepin County Medical CenterMinneapolisMinnesota55415-
Wake Forest Baptist Medical CenterWinston-SalemNorth Carolina27157-
Vanderbilt University Medical CenterNashvilleTennessee37203-

Find similar trials in Birmingham, AL

Related Studies