Feasibility Study: The Effect of Prazosin for Nighttime Symptoms of Civilian PTSD
NCT00174551 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2006-09-11
Summary
Investigating the effect of prazosin for nighttime symptoms of civilian Posttraumatic Stress Disorder.
Conditions
- Stress Disorders, Post-Traumatic
Interventions
- DRUG
-
prazosin
Sponsors & Collaborators
-
Rainier Associates
lead OTHER
Principal Investigators
-
Fletcher B Taylor, M.D. · Rainier Associates
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-11-30
- Completion
- 2005-11-30
Countries
- United States
Study Locations
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