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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT00215163 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Paroxetine-CR to Treat Post-Traumatic Stress Disorder (PTSD) Symptomatic After Initial Exposure Therapy

Start date: December 2002
Phase: Phase 2/Phase 3
Study type: Interventional

Both pharmacotherapeutic and psychosocial interventions have domenstrated efficacy for PTSD. However, although these interventions can be helpful, many patients remain symptomatic despite initial treatment. In this study, we will examine the relative efficacy of the addition of paroxetine-CR compared to placebo for patients remaining symptomatic despite a brief and intensive course of cognitive-behavioral therapy (CBT).

NCT ID: NCT00209040 Completed - Clinical trials for Posttraumatic Stress Disorder

Fear Potentiation and Fear Inhibition in Posttraumatic Stress Disorder

Start date: January 2001
Phase: N/A
Study type: Interventional

The current study will investigate the ability of people with and without fear symptoms after trauma to inhibit fear in an experimental situation.

NCT ID: NCT00208208 Completed - PTSD Clinical Trials

Geodon (Ziprasidone) for Posttraumatic Stress Disorder

Start date: December 2002
Phase: Phase 4
Study type: Interventional

Atypical antipsychotics have shown promise in the treatment of depression and anxiety, which are prominent symptoms of PTSD. The profile of the atypical antipsychotic, ziprasidone (Geodon), suggests possible anxiolytic and antidepressant properties. This research will assess the potential effectiveness of Geodon in civilian men and women who suffer from severe PTSD. Response to ziprasidone or placebo will be measured by Clinician Administered PTSD Scale (CAPS) and Treatment Outcomes PTSD Scale (TOP-8).

NCT ID: NCT00208182 Completed - Clinical trials for Post-Traumatic Stress Disorder

Risperidone in the Treatment of PTSD in Women Survivors of Domestic Abuse and Rape Trauma

Start date: July 2001
Phase: Phase 4
Study type: Interventional

This medical study is an assessment of clinical response in women with Posttraumatic Stress Disorder (PTSD) due to domestic violence or rape trauma when treated with risperidone. Response to risperidone or placebo (inactive drug) is measured by Clinician Administered PTSD Scale (CAPS) and Treatment Outcomes PTSD Scale (TOP-8). Second, the effect of risperidone on depressive and anxiety symptoms will be assessed using the Hamilton Rating Scale for Anxiety, Hamilton Rating Scale for Depression and the Clinical Global Impression.

NCT ID: NCT00208130 Completed - Clinical trials for Post-Traumatic Stress Disorder

Topiramate in the Treatment of Posttraumatic Stress Disorder in Civilians

Start date: October 2001
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to investigate the safety and efficacy of topiramate in the treatment of PTSD in women survivors of domestic violence and/or rape trauma as measured by the Clinician-Administered PTSD Scale (CAPS) for DSM-IV.

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: NCT00204386 Completed - Clinical trials for Posttraumatic Stress Disorder

Safety & Efficacy Study Using Topiramate in Posttraumatic Stress Disorder

Start date: September 2002
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study was to determine if Topiramate was safe and effective for use in civilian subjects with Posttraumatic Stress Disorder.

NCT ID: NCT00203463 Completed - PTSD Clinical Trials

Topiramate in the Treatment of Post Traumatic Stress Disorder (PTSD)

Start date: July 2001
Phase: Phase 4
Study type: Interventional

To study the potential therapeutic effects of topiramate (Topamax) in the treatment of PTSD.

NCT ID: NCT00186511 Completed - Breast Cancer Clinical Trials

Expanding Rural Access: Distance Delivery of Support

Start date: November 2004
Phase: Phase 2
Study type: Interventional

The major goal of this project is to test the feasibility and acceptability of using videoconferencing to provide support groups led by trained facilitators to rural women with breast cancer in northern California.

NCT ID: NCT00186472 Completed - Depression Clinical Trials

Intervention to Decrease Anxiety in Parents of Infants in the Neonatal Intensive Care Unit (NICU)

Start date: n/a
Phase: N/A
Study type: Interventional

Infants born premature face numerous medical problems, causing significant anxiety for their parents. Parents experience a range of negative emotions including concern for the health and well being of their fragile infant, guilt, and disappointment. Research has indicated that having an infant in the Neonatal Intensive Care Unit (NICU) is highly stressful for parents and multiple studies have demonstrated that parents can develop significant psychological reactions to this experience. Specifically, many parents develop clinically significant anxiety disorders such as acute stress disorder (ASD) and posttraumatic stress disorder (PTSD). This not only impacts the mental well-being of the parents, but also can lead to problems with the parent-infant relationship, and, in turn, negatively impact the infant and the family as a whole. Despite the reported negative effects parents experience due to the stress of having an infant on the NICU, surprisingly little research has examined how to reduce parents' symptoms of anxiety. Because parents play an essential role in the care of their infant after discharge from the NICU, treating the parent's emotional distress is highly important. The purpose of this study is to examine the efficacy of a cognitive-behaviorally based intervention in reducing parents' symptoms of anxiety associated with having an infant on the NICU. This treatment is modeled after treatments that have proven effective with parents of children with other types of medical problems, for example, parents of children with cancer. It is the hope of the investigators that this intervention will effectively reduce symptoms of anxiety of NICU parents as well as the likelihood of developing subsequent psychological disorders.