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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT00344682 Completed - Depressive Disorder Clinical Trials

Memantine Augmentation of Antidepressants

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

This study is evaluating the efficacy and safety of the drug memantine (trade name NAMENDA) as an augmentation agent for the treatment of depression in people who are not fully responding to antidepressant medications.

NCT ID: NCT00343707 Completed - Clinical trials for Depressive Disorder and Anxiety Disorders

PET (Positron Emission Tomography)/Public Speaking Study With A Combination Of 2 Medications In Social Anxiety Patients

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

This six-arm study is being conducted to measure the effect of a combination of paroxetine and vestipitant on the arousal induced by public speaking in Seasonal Effective Disorder (SAD) patients, using functional brain imaging readouts (i.e., WAT(Wave Analysis Technology) PET(Positron Emission Tomography)), after one or eight weeks of treatment. The effect of paroxetine alone after one or eight weeks of treatment will also be measured.

NCT ID: NCT00343070 Completed - Major Depression Clinical Trials

Functional Neuroimaging in Depression

Start date: March 2007
Phase: Phase 2
Study type: Interventional

Oral administration of escitalopram during 8 weeks; PET scan with 18F-FDG at inclusion and after 8 weeks

NCT ID: NCT00339066 Completed - Depression Clinical Trials

Effect of Brain Lesion Severity on Treatment Response in Late-Life Depression

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

This study will determine the relationship between brain lesion severity, treatment response, and frontal lobe brain function in people with late-life depression (LLD).

NCT ID: NCT00338962 Completed - Depression Clinical Trials

Naltrexone & SSRI in Alcoholics With Depression/PTSD

Start date: October 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of naltrexone in combination with an SSRI to reduce alcohol consumption in alcoholic patients with comorbid PTSD and depression. We hypothesize that the combination of naltrexone and SSRI will exhibit a greater decrease in alcohol consumption than that seen with treatment with SSRI alone, or with a combination of another class of antidepressant and naltrexone. We also hypothesize that SSRI will be effective in treating PTSD and depressive symptoms and naltrexone will be well tolerated.

NCT ID: NCT00336713 Completed - Depressive Disorder Clinical Trials

A 24-52-week Study to Evaluate the Long-term Efficacy and Safety of Saredutant in Patients With Depression (MAGENTA)

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

The purpose of the study is to evaluate the long-term efficacy and safety of saredutant in patients with depression. The primary objective is to evaluate the efficacy and safety of saredutant 100 mg once daily compared to placebo in the prevention of relapse of depressive symptoms in outpatients with major depressive disorder who achieved an initial response to 12 weeks of open-label treatment with saredutant.

NCT ID: NCT00331799 Completed - Clinical trials for Major Depressive Disorder

Pilot Study of Duloxetine in Psychological Resilience

Start date: April 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to explore benefits of duloxetine in enhancing psychological resilience and to understand the relevance of inhibiting of both serotonin (5HT) and norepinephrine (NE)to therapeutic responses.

NCT ID: NCT00331305 Completed - Depression Clinical Trials

Exercise Training Versus Drug Therapy for Treating Depression in Older Adults

Start date: August 1999
Phase: Phase 3
Study type: Interventional

This study will evaluate the effectiveness of both center-based and home-based exercise versus the antidepressant drug sertraline in treating depression in middle-aged and older adults.

NCT ID: NCT00330616 Completed - Clinical trials for Major Depressive Disorder (MDD)

Study Of Bupropion SR (323U66) In Patients With Major Depressive Disorder In Japan

Start date: May 2006
Phase: Phase 2
Study type: Interventional

This is a study to obtain clinical experience of 323U66 SR for elderly patients with depression in repeat-dose of 323U66 SR up to 300mg/day, and to conduct exploratory investigation on safety, efficacy and pharmacokinetics profile in elderly patients with depression.

NCT ID: NCT00330174 Completed - Alcohol Dependence Clinical Trials

Acamprosate in Alcoholics With Comorbid Anxiety or Depression

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

STUDY OBJECTIVES: The primary objective of this study is to compare the safety and efficacy of acamprosate versus placebo in the treatment of alcohol dependence in adults with co-occurring mood or anxiety disorders (specifically, depression (MDE), generalized anxiety disorder (GAD) or social anxiety disorder). Secondary objectives are to evaluate the effect of acamprosate treatment on mood and anxiety disorders. STUDY DESIGN: This is a randomized, double-blind, placebo-controlled trial evaluating acamprosate in the treatment of alcohol dependence in adult outpatients with concurrent mood and/or anxiety disorders. The active study phase will be 12 weeks in duration. There will be a two-week screening period, followed by 12 weeks of study medication and a follow-up assessment at 14 weeks from randomization. STUDY POPULATION: A total of 90 (30 per site) men and women aged 18-60 years who have a current diagnosis of alcohol dependence as well as a current DSM-IV diagnosis of either MDE, GAD and/or social anxiety will be recruited to participate in this study. Only those individuals whose psychiatric disorders are stable will be randomized to acamprosate or placebo. Three sites will participate in this trial. TREATMENTS: Eligible participants will be randomly assigned to receive either acamprosate or matching placebo for 12 weeks. EFFICACY ASSESSEMENTS: The primary efficacy outcome measure will be cumulative days abstinent as measured by self-report.