Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Utah
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Victim of a traumatic event leading to personal injury
Patient experienced a feeling of intense fear, hopelessness, or horror during the course of the event or immediately afterward
Positive screen on the ASDS (for inclusion in the randomization phase); a total ASDS score of ≥ 37 (including a dissociative score of ≥ 9) will be counted as a positive screen.
You may not be if
Age \< 18
Pregnant women, lactating women, or women not using acceptable form of birth control
Epilepsy or head trauma resulting in seizures
Current or historical schizophrenia, bipolar disorder, mental retardation, OCD, eating disorders, dementia, delirium, or self-injurious behavior
Current/previously diagnosed PTSD
History of hypersensitivity to sertraline
Trauma occurring \> 7 days prior to likely first treatment in the randomization phase of the trial.
Unable to provide informed consent for participation in the study protocol.
Patient at high risk of recurrent bleeding despite surgical stabilization
Patient with a history of serotonin syndrome
Patient non-fluent in English
Patient currently prescribed an antidepressant (any SSRI, SNRI, TCA, MAOI, mirtazapine, or trazodone in excess of 100mg per day)
Clareo Health | PTSD Prevention Study Examining the Efficacy of Sertraline in Burn Victims
