Reduction of nightmares and other PTSD symptoms in combat veterans by prazosin: a placebo-controlled study
- PMID: 12562588
- DOI: 10.1176/appi.ajp.160.2.371
Reduction of nightmares and other PTSD symptoms in combat veterans by prazosin: a placebo-controlled study
Abstract
Objective: Prazosin is a centrally active alpha(1) adrenergic antagonist. The authors' goal was to evaluate prazosin efficacy for nightmares, sleep disturbance, and overall posttraumatic stress disorder (PTSD) in combat veterans.
Method: Ten Vietnam combat veterans with chronic PTSD and severe trauma-related nightmares each received prazosin and placebo in a 20-week double-blind crossover protocol.
Results: Prazosin (mean dose=9.5 mg/day at bedtime, SD=0.5) was superior to placebo for the three primary outcome measures: scores on the 1) recurrent distressing dreams item and the 2) difficulty falling/staying asleep item of the Clinician-Administered PTSD Scale and 3) change in overall PTSD severity and functional status according to the Clinical Global Impression of change. Total score and symptom cluster scores for reexperiencing, avoidance/numbing, and hyperarousal on the Clinician-Administered PTSD Scale also were significantly more improved in the prazosin condition, and prazosin was well tolerated.
Conclusions: These data support the efficacy of prazosin for nightmares, sleep disturbance, and other PTSD symptoms.
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