Skip to content
Enrolling by invitationN/A

Effect of Ketamine and Etomidate During RSI on Long Term Outcomes

NCT06179485 · RSI-LTO · Vanderbilt University Medical Center

Closed to entry
Status
Not accepting participants
Not applicable
Phase
1,756
Target enrolment
6
Study sites
5 US states

What it is testing

Summary

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.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • PTSD Symptoms at 12 months

    Measured over 12 months

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Enrolled in RSI trial (NCT05277896) Exclusion Criteria: * Aphasic or non-verbal prior to tracheal intubation * Cannot follow commands prior to tracheal intubation * Non-English speaking * Deaf

Where

6 study sites

FacilityCityRegionCountry
University of Alabama HospitalBirminghamAlabamaUnited States
University of Colorado DenverAuroraColoradoUnited States
Denver Health Medical CenterDenverColoradoUnited States
Hennepin County Medical CenterMinneapolisMinnesotaUnited States
Wake Forest Baptist Medical CenterWinston-SalemNorth CarolinaUnited States
Vanderbilt University Medical CenterNashvilleTennesseeUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT06179485 on ClinicalTrials.gov →

Last updated in the registry 2026-08-20. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits