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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT00735995 Completed - Clinical trials for Generalized Anxiety Disorder

Effectiveness of Cognitive Behavioral Therapy (CBT) for Child Anxiety Disorders in Community Clinics in Norway

Start date: August 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effectiveness of a cognitive-behavioral intervention for children aged 7 to 12 years with anxiety disorders who are referred to ordinary community clinics. The treatment will be conducted as individual therapy or group therapy.

NCT ID: NCT00735267 Terminated - Clinical trials for Generalized Anxiety Disorder

A 52-Week Open-Label Safety Study of PD 0332334 in Subjects With Generalized Anxiety Disorder (GAD)

Start date: October 2008
Phase: Phase 3
Study type: Interventional

This study will assess the long-term safety and tolerability of 350 to 600 mg/day of PD 0332334 administered in split dose (twice daily) in subjects with Generalized Anxiety Disorder.

NCT ID: NCT00734071 Completed - Clinical trials for Generalized Anxiety Disorder

An Efficacy and Safety Study of Vortioxetine (Lu AA21004) in Treating Generalized Anxiety Disorder

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of vortioxetine, once daily (QD), in treating Generalized Anxiety Disorder.

NCT ID: NCT00731120 Completed - Clinical trials for Generalized Anxiety Disorder

Study of Efficacy and Safety of Vortioxetine (Lu AA21004) in Treating Generalized Anxiety Disorder

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of 2.5 mg and 10 mg vortioxetine, once daily (QD), in adults with generalized anxiety disorder.

NCT ID: NCT00730691 Completed - Clinical trials for Generalized Anxiety Disorder

Efficacy of Vortioxetine (Lu AA21004) in Treating Generalized Anxiety Disorder

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of vortioxetine, once daily (QD), in adults with generalized anxiety disorder.

NCT ID: NCT00721526 Completed - Alcohol Dependence Clinical Trials

Disulfiram Combined With Lorazepam for Alcohol Dependence and Anxiety Disorder

Start date: August 2009
Phase: Phase 4
Study type: Interventional

The proposed design is a single-group open-label trial. Qualified consenting participants with active alcohol dependence and primary or secondary anxiety disorder will receive monitored disulfiram and lorazepam, in the context of a structured Medication Management (MM) model. In weeks 9-15 lorazepam is tapered, and disulfiram is stopped at the end of week 16. Participants who achieve 4 weeks abstinence and meet criteria for a primary anxiety disorder or mood disorder may receive ancillary medication consisting FDA-approved non-benzodiazepine treatment, with specific options for each disorder described in the protocol. Participants requiring continued treatment are referred to clinical treatment in the community at week 16, and bridging prescriptions of anxiolytic/antidepressant medication may be provided. A final follow-up assessment occurs at week 28. The primary outcomes are Percent Days Abstinent (PDA) and retention in treatment. Secondary alcohol outcomes are consequences, drinks per drinking day, remission status, and time to first heavy drinking day. Anxiety outcomes are Hamilton Anxiety Scale scores and anxiety disorder diagnosis.

NCT ID: NCT00717041 Completed - Depression Clinical Trials

Epidemiology of Depression, Anxiety, and Cognitive Impairment

Start date: May 2008
Phase: N/A
Study type: Observational

Many older adults have undetected health problems and lack basic prevention measures. Failure to identify and treat these conditions can lead to unnecessary morbidity and mortality and a decreased quality of life. Traditional screening and intervention programs, usually based in primary care providers' offices, have been insufficient, particularly in medically underserved populations. Alternate sites for screening and intervention have begun to receive attention and may hold promise. The emergency department (ED) is the entry point for access to medical and social services for many patients and has the potential to serve as a site to identify older adults with unmet needs. However, we do not know the prevalence of depression and cognitive impairment and how they differ by mode of arrival of the patient to the ED. Second, a question remains as to the validity of screening patients during an acute illness. Upon completion, this study will describe the epidemiology of the population of older adults presenting to the ED.

NCT ID: NCT00715039 Completed - Anxiety Disorders Clinical Trials

Clinical Study Assessing a New Scale to Measure Onset of Action in Generalized Anxiety Disorder

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

The study is to assess the performance characteristics of a new measure to assess onset of efficacy in a GAD patient population.

NCT ID: NCT00711737 Completed - Clinical trials for Generalized Anxiety Disorder

Study of the Changes in Metabolic Parameters in Patients Treated With Escitalopram for Six Months

Start date: September 2008
Phase: N/A
Study type: Observational

The purpose of this study is to explore the changes in metabolic parameters in patients treated with escitalopram for six months for major depression, generalized anxiety disorder or panic disorder, with or without agoraphobia.

NCT ID: NCT00706836 Completed - Anxiety Disorders Clinical Trials

PharmacofMRI of Anxiolytic Medications (Pregabalin)

Start date: June 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to use functional magnetic resonance imaging (fMRI) in healthy controls to examine the acute effects of certain anxiolytic medications on brain function. In this case, the medication pregabalin will be used. The investigators hypothesize that pregabalin (at doses of 50 mg and 200 mg, versus placebo) will yield a reduction in amygdala and insula activity (in a dose-dependent fashion) during emotion processing using fMRI.