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Generalized Anxiety Disorder clinical trials

View clinical trials related to Generalized Anxiety Disorder.

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NCT ID: NCT00322595 Completed - Clinical trials for Generalized Anxiety Disorder

Efficacy and Safety Study of Seroquel SR in the Treatment of Generalized Anxiety Disorder

SILVER
Start date: May 2006
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy of (SEROQUEL SR™ ) quetiapine fumarate sustained-release (SR) compared to placebo in the treatment of anxiety symptoms in patients with generalized anxiety disorder (GAD). PLEASE NOTE: Seroquel SR and Seroquel XR refer to the same formulation. The SR designation was changed to XR after consultation with FDA.

NCT ID: NCT00308724 Completed - Clinical trials for Generalized Anxiety Disorder

Treating Late-Life Generalized Anxiety Disorder (GAD) in Primary Care

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

The purpose of this study is to determine whether cognitive behavior therapy (CBT) is effective in the treatment of generalized anxiety disorder (GAD) in adults age 60 and older in a primary care setting.

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: NCT00236067 Completed - Clinical trials for Generalized Anxiety Disorder

A 10-Week Study for Efficacy and Safety Study of Gabitril in the Treatment of Adults With Generalized Anxiety Disorder

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

The purpose of this study is to evaluate the safety and efficacy of an investigational anti-anxiety medication relative to placebo in patients with generalized anxiety disorder (GAD).

NCT ID: NCT00236054 Completed - Clinical trials for Generalized Anxiety Disorder

A 10-Week Efficacy and Safety Study for of Gabitril in the Treatment of Adults With Generalized Anxiety Disorder

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

The purpose of this study is to evaluate the safety and efficacy of an investigational anti-anxiety medication relative to placebo in patients with generalized anxiety disorder (GAD)

NCT ID: NCT00235508 Completed - Insomnia Clinical Trials

Safety and Efficacy of Eszopiclone in Patients With Generalized Anxiety Disorder

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

To determine the safety and efficacy of eszopiclone as adjunctive therapy in the treatment of insomnia in patients with insomnia related to Generalized Anxiety Disorder. All subjects will receive an approved anxiolytic agent and will be randomized to nightly therapy with either eszopiclone or placebo.

NCT ID: NCT00219349 Completed - Clinical trials for Generalized Anxiety Disorder

Cognitive-Behavioral Therapy and Escitalopram for Generalized Anxiety Disorder(GAD)

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

The goals of this pilot study are as follows: 1) To disseminate and examine the effectiveness of a manualized, individual, cognitive-behavioral psychotherapy (CBT) for adults with Generalized Anxiety Disorder(GAD), 2) to test the effectiveness of augmentation (the addition of) antidepressant therapy in participants who do not fully respond to CBT, and 3) to examine individual and clinical predictors of non-response to CBT and predictors of response to augmentation antidepressant therapy. A related goal is to examine the maintenance of treatment gains obtained from CBT alone and CBT with augmentation antidepressant therapy, over a twenty-four month follow-up period. This study will serve as a pilot investigation in preparation for a larger federally funded study using this treatment approach. We hypothesize that CBT will result in remission (no longer having GAD) and/or high endstate functioning (clinically meaningful improvement) in approximately 40-50% of participants. Further, we hypothesize that augmentation antidepressant therapy in participants who do not fully respond to CBT will result in further clinically significant improvement.

NCT ID: NCT00208910 Completed - Anxiety Clinical Trials

Muscle Relaxation Therapy With Odorant Cue

Start date: November 2003
Phase: N/A
Study type: Interventional

A novel procedure for generalized anxiety disorder where an odorant cue is paired with the state of deep relaxation during training. It is hypothesized that by smelling the odor in an anxiety-provoking situation, the patient will more easily invoke a state of relaxation, providing greater relief from the distressing tension and worry that characterize GAD.

NCT ID: NCT00167479 Completed - Bipolar Disorder Clinical Trials

A Study of Risperidone Monotherapy in Bipolar Anxiety

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

The specific aim of this study is to evaluate the efficacy, tolerability, and safety of risperidone monotherapy in the treatment of ambulatory bipolar disorder with comorbid lifetime panic disorder or generalized anxiety disorder and current at least moderately severe anxiety.

NCT ID: NCT00141115 Completed - Anxiety Disorders Clinical Trials

Levetiracetam for the Treatment of Alcohol Dependence and Anxiety

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

The purpose of this study is to determine if levetiracetam is effective in treating alcohol dependence in patients with anxiety symptoms. The researchers hypothesize that individuals are unable to reduce or discontinue alcohol use because of significant anxiety, mood, and sleep disturbance symptoms that accompany reduction in alcohol use.