ED Treatment of Suicidal Patients With Ketamine Infusion
Withdrawn before enrolling · Phase 2
Conditions studied: Suicide, Suicidal Ideation
In brief
This study aims to determine if a single intravenous (IV) dose of ketamine given in the emergency department (ED) can provide a long term reduction in suicidal ideation, lower time to ED discharge, and increase discharge to home or voluntary treatment facilities all while being safe.
Key facts
- Study ID
- NCT03502551
- Run by
- University of California, Davis
- People needed
- 0
- Starts
- 2019-04-01
- Expected to finish
- 2019-06-30
- Last updated by the study team
- 2019-05-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years
- Chief complaint of suicidal thoughts with a MADRS-SI score > 3
- Major depressive episode with MADRS > 19 (moderate to severe)
You may not qualify if…
- Pregnancy
- Psychosis
- Acute intoxication with alcohol or illicit drugs
- Acute withdrawal from alcohol or illicit drugs
- Adults otherwise unable to consent
- Concurrent, active medical illness requiring medical hospitalization
- Inability to follow-up including no permanent address or valid telephone number
- Patients unable to attend outpatient follow-up (no medical insurance, refusal to follow-up, no established care provider)
- Specific contraindication to the use of ketamine (concern for increased intracranial or intraocular pressure, known allergy to ketamine)
- Greater than 12 hours from time of ED presentation
- Prisoners
Where it is running
- University of California Davis Medical Center — Sacramento, California, United States
Full record on ClinicalTrials.gov
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