Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00890643

Effect of Prazosin on Neurophysiology and Cognition in Post-Traumatic Stress Disorder (PTSD)

Effect of Prazosin on Neurophysiologic Responses and Cognitive Performance in PTSD

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
US Department of Veterans Affairs · Federal
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

In this study, the investigators are looking at how PTSD affects things such as memory, attention, reaction to sounds, eye movements, and heart rate. The investigators are also studying whether a medication called prazosin has an effect on these things.

Detailed description

Converging lines of evidence suggest that central nor adrenergic function is perturbed in PTSD. Placebo-controlled trials demonstrate that the centrally acting alpha-1 antagonist prazosin is clinically effective for several core symptoms of PTSD in combat veterans. However, no detailed assessment of the impact of prazosin on human neurophysiology and cognition have been conducted. Our hypotheses are based on studies that demonstrate (1) the importance of central adrenergic receptors in regulating fundamental neurophysiologic and cognitive functions, (2) the alteration of these functions in PTSD, and (3) the efficacy of prazosin in improving the clinical symptoms of PTSD. The primary objective of this study is to measure the subtle neurocognitive and neurophysiologic effects on prazosin in combat veterans with PTSD.

Conditions

Interventions

TypeNameDescription
DRUGprazosin hydrochlorideprazosin 1-20 mg/day in divided doses
DRUGplaceboplacebo

Timeline

Start date
2009-12-01
Primary completion
2011-06-01
Completion
2011-09-01
First posted
2009-04-30
Last updated
2013-09-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00890643. Inclusion in this directory is not an endorsement.