Clinical Trials Logo

Posttraumatic Stress Disorder clinical trials

View clinical trials related to Posttraumatic Stress Disorder.

Filter by:

NCT ID: NCT00353938 Completed - Clinical trials for Posttraumatic Stress Disorder

Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder

Start date: September 13, 2006
Phase: Phase 2
Study type: Interventional

This study will examine MDMA-assisted psychotherapy in individuals aged 18 years or older diagnosed with PTSD, with PTSD symptoms not improving after trying at least one treatment. This objective of this study is to determine whether three eight-hour long sessions of MDMA-assisted psychotherapy, scheduled three to five weeks apart, can be safely administered to participants with PTSD, and whether combining a fully therapeutic dose of MDMA with psychotherapy, when compared with a low ("active placebo") dose of MDMA, will reduce PTSD symptoms. Participants will be randomly assigned to receive the full dose of MDMA (125 mg) or assigned to receive a low or "active placebo" dose of MDMA (25 mg) during each of three experimental sessions.

NCT ID: NCT00290225 Completed - Depression Clinical Trials

Yoga Breath Program and Client-Centered Exposure for Relief of PTSD in Tsunami Victims

Start date: June 2005
Phase: Phase 3
Study type: Interventional

Study hypothesis: that a standardized course of Eastern practices (Breath Water Sound Course -BWS) will significantly relieve PTSD and depression in tsunami victims. Further, that a client-centered exposure treatment (Traumatic Incident Reduction- TIR) would provide additional, significant relief of PTSD and depression in tsunami victims. 180 tsunami victims in Southern India will be divided into three groups: those that only receive BWS course, those that receive the BWS course and TIR and a wait-list control. They will be pretested with the PCL-17 (PTSD scale), the Beck Depression Inventory and the General Health Questionaire. These scales will also be administered post-service as well as five weeks post pre-testing and at three and six month intervals.

NCT ID: NCT00265564 Completed - Clinical trials for Posttraumatic Stress Disorder

SUPER Study (Substance Use and PTSD Treatment Effectiveness Research Study)

Start date: July 2006
Phase: N/A
Study type: Interventional

This study proposes a prospective program of research that will identify feasible and inexpensive methods to detect and treat comorbid PTSD among VA SUD patients, thereby improving substance abuse treatment outcomes.

NCT ID: NCT00256477 Completed - Clinical trials for Posttraumatic Stress Disorder

A Controlled Breathing Course for Social & Emotional Health for Vietnam Veterans With Chronic PTSD-RCT

Start date: March 2005
Phase: Phase 1
Study type: Interventional

The main aim of this project is to evaluate the use of a specific Yoga technique of controlled breathing in Vietnam War Veterans with chronic posttraumatic stress disorder. This method is currently the subject of a United States grant application to formally test American War Veterans from Afghanistan and Iraq. Drs Gerbarg and Brown are collaborating with The Bay Pines Veterans Administration Medical Center in Florida to develop a study of this course for treatment of American veterans returning from Afghanistan and Iraq. Elements of this method have been used on a variety of populations. Whilst this is a multi-component intervention, it is postulated that the most active ingredient in the program is a specific Yoga breathing technique called Sudarshan Kriya (SK).

NCT ID: NCT00229372 Completed - Clinical trials for Posttraumatic Stress Disorder

Prolonged Exposure Versus Treatment as Usual in Chronic Posttraumatic Stress Disorder Combat and Terror Related Patients

Start date: November 2006
Phase: N/A
Study type: Interventional

Assessing the efficacy of Posttraumatic Stress Disorder (PE) treatment for chronic Posttraumatic Stress Disorder (PTSD)

NCT ID: NCT00229294 Completed - Clinical trials for Major Depressive Disorder

Fibromyalgia in Men Suffering From PTSD

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

Assessing FM and psychiatric state among PTSD, MDD and healthy participants

NCT ID: NCT00218959 Completed - Clinical trials for Posttraumatic Stress Disorder

Randomized Controlled Trial of Narrative Exposure Therapy Compared to Treatment as Usual for Traumatized Refugees

Start date: September 2005
Phase: N/A
Study type: Interventional

In this study we want to compare Narrative Exposure Therapy to Treatment as Usual for traumatized refugees and asylum seekers in the Mid- Norway region. Clinicians in psychiatric outpatient clinics will deliver the two conditions to asylum seekers and refugees that qualifies for Posttraumatic Stress Disorder. We will investigate if refugees and asylum seekers will improve more with Narrative Exposure Therapy or Treatment as Usual, and if there will be any differences between improvement for asylum seekers compared to improvement for refugees with residential status.

NCT ID: NCT00215878 Completed - Clinical trials for Posttraumatic Stress Disorder

D-serine for Posttraumatic Stress Disorder Treatment

Start date: August 2003
Phase: Phase 2
Study type: Interventional

The aim of this study is to asses the effects of the NMDA receptor full agonist D-serine while used as adjuvant treatment for individuals suffering from chronic posttraumatic stress disorder (PTSD). Dysfunction of neurotransmission mediated at NMDA receptor plays a cardinal role in the pathophysiology of PTSD and PTSD patients typically suffer from cognitive dysfunctions and avoidance& depressive symptomatology that may be mediated by NMDA receptor function deficits. Thus, enhancement of NMDA activity by using D-serine may be beneficial in the treatment of PTSD. The study design involves two 6 week periods during which the participants will be randomly assigned to receive treatment with D-serine (~2g /dy)and placebo. This design allows each participant the opportunity to respond to the experimental treatment.

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).