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Panic Disorder clinical trials

View clinical trials related to Panic Disorder.

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NCT ID: NCT00456768 Completed - Panic Disorder Clinical Trials

Efficacy of Treatment for Panic Disorder

Start date: May 2003
Phase: N/A
Study type: Observational

The purpose of these questionnaires is to give us an overview of how panic has affected your life and perhaps also to give us some clues about things that may have set you up to experience panic.

NCT ID: NCT00438971 Completed - Panic Disorder Clinical Trials

The Efficacy and Tolerability of Duloxetine for the Treatment of Panic Disorder

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether duloxetine is effective in the treatment of panic disorder.

NCT ID: NCT00438386 Completed - Clinical trials for Generalized Anxiety Disorder

Aripiprazole for the Treatment of Refractory Anxiety

Start date: April 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether aripiprazole is effective in the treatment of refractory panic and generalized anxiety disorder.

NCT ID: NCT00353470 Completed - Anxiety Disorders Clinical Trials

Comparison of Psychotherapy Programs to Treat Panic Disorder

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This study will determine the relative effectiveness of three psychotherapies in treating people with a panic disorder.

NCT ID: NCT00352469 Completed - Anxiety Disorders Clinical Trials

Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety

Start date: February 2006
Phase: Phase 4
Study type: Interventional

Alcohol use disorders (AUDs) are a major problem facing our society. Their treatment is complex, and involves multiple behavioral and pharmacotherapy interventions. There are 3 approved medications for AUDs, but their efficacy for AUDs that co-exist with anxiety disorders is unknown. This study explores the effects of the medication, sustained-release quetiapine fumarate (Seroquel SR) for the treatment of alcohol dependence and co-morbid anxiety. Primary outcome measure is the amount of alcohol used. Secondary outcome measures include craving for alcohol, length of sobriety from drinking and level of anxiety with Seroquel SR.

NCT ID: NCT00347269 Completed - Clinical trials for Post-traumatic Stress Disorder

Primary Care Intervention Strategy for Anxiety Disorders

Start date: June 2006
Phase: Phase 4
Study type: Interventional

This study will compare the effectiveness of an intervention strategy for the treatment of people with post traumatic stress disorder, generalized anxiety disorder, panic disorder, and social anxiety disorder in the primary care setting.

NCT ID: NCT00344474 Completed - Depression Clinical Trials

Personality-targeted Interventions for Adolescent Alcohol Misuse

Preventure
Start date: November 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Personality targeted cognitive behavioural interventions have been shown to be effective in reducing alcohol and drug misuse in adult substance abusers (Conrod et al., 2000) and adolescent drinkers (Conrod et al, in press). As these interventions target personality traits linked to risk for addictive and non-addictive mental disorders, the aim of this study is to examine the extent to which this approach can prevent and/or reduce alcohol and drug misuse as well as have an impact on the onset or severity of emotional and behavioural problems in young people.

NCT ID: NCT00279617 Completed - Panic Disorder Clinical Trials

Levetiracetam Treatment of Panic Disorder and Lactate-Induced Panic Attacks

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The main purpose of this research study is to determine whether the drug Levetiracetam (Keppra™) is effective in the prevention of panic attacks. The drug Levetiracetam (Keppra™) has been approved for the treatment of seizures by the U.S. Federal Food and Drug Administration (FDA) and is available by prescription. Levetiracetam has not been approved by the FDA for the treatment of panic disorder.

NCT ID: NCT00266409 Completed - Clinical trials for Generalized Anxiety Disorder

Trial to Compare Time to Response in the Symptoms of Anxiety to Concomitant Treatment With Niravam™ and an SSRI or SNRI to Treatment With an SSRI or SNRI Alone in Subjects With Generalized Anxiety Disorder or Panic Disorder

Start date: October 2005
Phase: Phase 4
Study type: Interventional

An 8-week, open-label trial in 848 subjects at 212 sites to compare time to response in symptoms of anxiety in subjects treated with Niravam™ and a newly prescribed Selective Serotonin Reuptake Inhibitor (SSRI)or Serotonin and Norepinephrine Reuptake Inhibitor (SNRI) to that in subjects treated with a newly prescribed SSRI/SNRI alone. Subjects must be at least 18 years of age and positive for Generalized Anxiety Disorder (GAD)or Panic Disorder. Subjects will be randomized to receive concomitant Niravam™ and an SSRI/SNRI or an SSRI/SNRI alone during the study. Most symptom evaluations will be done using an automated phone interview system. There are 4 clinic visits.

NCT ID: NCT00198094 Completed - Panic Disorder Clinical Trials

A Study of Sertraline and Early Alprazolam XR Administration Versus Sertraline Only in Panic Disorder Patients

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The primary objective for the study is to test the hypothesis that sertraline plus alprazolam XR will result in superior early stabilization of primary care PD patients versus sertraline/placebo over a 12-week treatment period. The secondary objectives of the study are a) to assess withdrawal symptoms during alprazolam XR taper (weeks 5-7 of the 12-week trial) and after discontinuation, b) to compare physical health outcomes, medical services utilization, and cost-effectiveness of the two study interventions across the 12-week treatment period and subsequent three month maintenance treatment with sertraline alone, and c) to assess whether early co-administration of sertraline/ alprazolam XR will result in greater maintenance of treatment response than sertraline/placebo over the three months following the 12 week acute treatment program.