Preventing Depression in People Receiving Mechanical Ventilation in an Intensive Care Unit
Completed · Phase 4 · Has a placebo group
Conditions studied: Depression
In brief
This study will determine the effectiveness of antidepressant medication in preventing depression and improving recovery in people who have been supported by mechanical ventilators in an intensive care unit (ICU).
Key facts
- Study ID
- NCT00872027
- Run by
- University of Minnesota
- People needed
- 15
- Starts
- 2009-04-01
- Expected to finish
- 2011-07-01
- Last updated by the study team
- 2017-12-19
Who can join
Age: 25 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Newly mechanically ventilated via an endotracheal tube
- Expected to remain intubated for at least 48 hours
- Fluent in English or Spanish
You may not qualify if…
- Depression before admission to the ICU, as determined by a proxy interview
- Use of antidepressant medication within the last 2 weeks or a monoamine oxidase (MAO) inhibitor in the previous month
- History of suicide attempt
- Ventricular arrhythmias or a seizure requiring medication in the last 6 months
- History of retinal vascular proliferation or bleeding
- Migraine headaches treated with 5-HT1 agonists
- Organ transplant within the last 6 months
- Score of less than 4 on the Glasgow coma scale, in the absence of drug effects, for 2 days
- Acute brain hemorrhage
- Increased intracranial pressure
- Active bleeding or less than 20,000 platelets/ul
- Expected prolonged inability to enterally administer escitalopram
- Residence more than 75 miles from study facility
- Serum sodium less than 125 mEq/l
- Hypersensitivity to citalopram or escitalopram
- Pregnant, breastfeeding, or possibly becoming pregnant in the next 3 months
- Undergoing life-support withdrawal or very low likelihood of 2-month survival
- Cognitive or communication impairment severe enough to preclude a conversation with an interviewer present before admission to ICU
Where it is running
- University of Minnesota Medical Center — Minneapolis, Minnesota, United States
Full record on ClinicalTrials.gov
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