Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | prazosin hydrochloride | prazosin 1-20 mg/day in divided doses |
| DRUG | placebo | placebo |
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.