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Post-Traumatic Stress Disorder clinical trials

View clinical trials related to Post-Traumatic Stress Disorder.

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NCT ID: NCT00204737 Completed - Clinical trials for Post-traumatic Stress Disorder

Short Course Glucocorticoid Treatment for PTSD

Start date: December 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate if a 2-wk course of 20mg/day of oral prednisone in addition to standard care will result in reduced PTSD symptoms or symptom severity compared to placebo

NCT ID: NCT00183716 Completed - Depression Clinical Trials

The Trauma Recovery and Empowerment Model for Treating Post-Traumatic Stress Disorder in Women

TREM
Start date: April 2004
Phase: Phase 3
Study type: Interventional

This study will determine the effectiveness of the Trauma Recovery and Empowerment Model in reducing the severity of post-traumatic stress disorder symptoms in women with mental disorders and who have experienced sexual or physical abuse.

NCT ID: NCT00183690 Completed - Clinical trials for Post-Traumatic Stress Disorder

Prolonged Exposure Therapy Versus Active Psychotherapy in Treating Post-Traumatic Stress Disorder in Adolescents

Start date: September 2004
Phase: Phase 1
Study type: Interventional

This study will compare the effectiveness of prolonged exposure therapy versus active psychotherapy in treating post-traumatic stress disorder (PTSD) in adolescents.

NCT ID: NCT00183300 Completed - Clinical trials for Post-Traumatic Stress Disorder

Relationship Between the Biological and Psychological Correlates of PTSD

Start date: September 2001
Phase: Phase 2
Study type: Interventional

This study will determine the effectiveness of immediate treatment with prolonged exposure therapy (PE) versus delaying treatment with PE in altering neuroendocrine-related symptoms of post-traumatic stress disorder in women.

NCT ID: NCT00166075 Completed - Depression Clinical Trials

Mental Health Symptoms and Intimate Partner Violence

Start date: January 2004
Phase: N/A
Study type: Observational

Using a touch screen computer, the researchers are screening emergency department patients for intimate partner violence and mental health issues.

NCT ID: NCT00158262 Completed - Clinical trials for Post-Traumatic Stress Disorder

Effect of Propranolol on Preventing Posttraumatic Stress Disorder

Start date: September 2004
Phase: Phase 4
Study type: Interventional

This study will assess the effectiveness of taking propranolol soon after a traumatizing incident in reducing the incidence and severity of posttraumatic stress disorder in acutely traumatized individuals.

NCT ID: NCT00146900 Completed - Clinical trials for Post-traumatic Stress Disorder

Prevention of Post Traumatic Stress Disorder by Early Treatment

Start date: August 2004
Phase: N/A
Study type: Interventional

To prospectively evaluate the effect of early treatment (cognitive therapy (CT), cognitive-behavioral therapy (CBT) and escitalopram (SSRI) in preventing the occurrence of post-traumatic stress disorder in recent survivors of traumatic events.

NCT ID: NCT00127673 Completed - Clinical trials for Post-Traumatic Stress Disorder

Comparison of Two Treatments for Post-Traumatic Stress Disorder

Start date: September 2004
Phase: Phase 3
Study type: Interventional

This study will compare the short- and long-term effectiveness of two different treatments for people with post-traumatic stress disorder.

NCT ID: NCT00108628 Completed - Clinical trials for Post-traumatic Stress Disorder

Cognitive Behavioral Treatments for Post-traumatic Stress Disorder (PTSD) Sleep Disturbance

Start date: April 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness of two cognitive behavioral group psychotherapy interventions in controlling the subjective sleep disturbance in veterans with Post-traumatic Stress Disorder.

NCT ID: NCT00102102 Completed - Clinical trials for Post-Traumatic Stress Disorder

Role of Substance P in Post-Traumatic Stress Disorder

Start date: January 2005
Phase: N/A
Study type: Observational

This study will examine the role of substance P, a chemical messenger in the brain, in post-traumatic stress disorder (PTSD), a chronic anxiety disorder. PTSD can develop after exposure to a terrifying event or ordeal, such as a violent personal assault, natural or human-caused disaster, accident, or military combat. Substance P is a peptide that may be important in the response to certain psychiatric and neurological diseases and conditions, including anxiety. Healthy normal volunteers and people with PTSD who are between 18 and 65 years of age may be eligible for this study. Candidates are screened with a physical examination, blood and urine tests, pregnancy test for women who can become pregnant, and a neuropsychological evaluation. Participants undergo positron emission tomography (PET) and magnetic resonance imaging (MRI) scanning. An optional lumbar puncture (spinal tap) is also requested. PET Scanning PET uses small amounts of a radioactive chemical called a tracer that "labels" active areas of the brain. The tracer used in this study is [18F]SPA-RQ. For the procedure, the subject lies still on the scanner bed. A special mask is fitted to the head to help keep the subject's head still during the scan so the images will be clear. A 20-minute "transmission" scan is done before the radioactive tracer is injected to provide measures of the brain that will help in the precise calculation of information from subsequent scans. After the tracer is injected through a needle in the arm, pictures are taken continuously for about 2 hours. Then, 20- to 40-minute images are taken every hour until about 5 hours after the injection. MRI Scanning An MRI scan is scheduled at some time within 1 year of the PET scan. MRI uses a magnetic field and radio waves to obtain images of body tissues and organs. The subject lies still on a table inside the tunnel-like MRI scanner. Earplugs are worn to muffle loud noises that occur during the scanning. The maximum duration of the scan is 60 minutes. Lumbar Puncture Lumbar puncture is used to examine the cerebrospinal fluid (CSF) that surrounds both the brain and the spinal cord. For this procedure, a local anesthetic is given to numb the skin in the lower back area. A small needle is then inserted into the space between the bones in the lower back where the CSF circulates below the spinal cord. A small amount of fluid is collected through the needle. Blood Draw A blood sample is collected to generate cell lines that can be used to extract DNA (genetic material) for gene studies and that can be frozen for future use.