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Clinical Trial Summary

Patients with PTSD, and frequent nightmares, and mild-moderate suicidal ideation, who are already taking a Selective Serotonin Reuptake Inhibitor (SSRI) or Serotonin Norepinephrine Reuptake Inhibitor (SNRI) will be randomized to either prazosin or placebo. The investigators hypothesize that patients receiving prazosin will have a greater reduction in suicidal ideation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02199652
Study type Interventional
Source Augusta University
Contact
Status Completed
Phase Phase 4
Start date March 2014
Completion date December 1, 2017

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