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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT00178100 Completed - Unipolar Depression Clinical Trials

Paroxetine and Interpersonal Psychotherapy for Maintaining Health and Well-being in Elderly Individuals With Depression

Start date: March 1999
Phase: Phase 4
Study type: Interventional

This study will evaluate the effectiveness of paroxetine versus interpersonal psychotherapy and a combination of the two in helping elderly patients with depression remain well and improve quality of their lives.

NCT ID: NCT00178087 Completed - Clinical trials for Late-Life Depression

Determining Changes in Brain Structure Associated With Symptoms of Late-life Depression

Start date: August 2005
Phase: N/A
Study type: Observational

This study will determine the changes in brain structure and function that are responsible for mood and cognition changes that are sometimes associated with late-life depression.

NCT ID: NCT00178074 Completed - Unipolar Depression Clinical Trials

The Effects of Sleep Deprivation on Antidepressant Response

Start date: February 1999
Phase: Phase 4
Study type: Interventional

This study will use positron emission tomography (PET) to examine the effect of sleep deprivation on brain function.

NCT ID: NCT00178035 Completed - Depression Clinical Trials

Sleep Deprivation Plus Paroxetine for Treating Major Depression in Elderly Individuals

Start date: December 1999
Phase: Phase 4
Study type: Interventional

This study will determine the effectiveness of total sleep deprivation (TSD) for one night plus paroxetine versus either TSD plus placebo or paroxetine alone in inducing rapid symptom resolution of major depression in the elderly.

NCT ID: NCT00177996 Completed - Major Depression Clinical Trials

Pharmacotherapy in Depression With Panic Spectrum

Start date: October 2001
Phase: Phase 4
Study type: Interventional

This research study is being conducted to find out if certain individuals benefit from taking medication for their depression with a low dose of the antidepressant medication Zoloft.

NCT ID: NCT00177671 Completed - Depression Clinical Trials

Antidepressant Medication Plus Donepezil for Treating Late-life Depression

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

This study will determine the effectiveness of combining escitalopram, venlafaxine, or duloxetine with donepezil, a medication used in Alzheimer's disease, in improving memory, concentration, attention, and problem solving abilities, and reducing the risk of depressive relapse in older individuals with depression.

NCT ID: NCT00177528 Completed - Depression Clinical Trials

Safety and Efficacy of Venlafaxine XR in Elderly Patients With Major Depression

Start date: October 2000
Phase: Phase 4
Study type: Interventional

This research study is to evaluate the safety and usefulness of venlafaxine-XR in the treatment of major depression in the elderly.

NCT ID: NCT00177294 Completed - Depression Clinical Trials

Augmenting Antidepressant Treatment With Interpersonal Psychotherapy for Treating Late-life Depression

Start date: April 2004
Phase: Phase 4
Study type: Interventional

This study will determine whether adding interpersonal psychotherapy to treatment with the antidepressant escitalopram will be more effective in reducing symptoms of depression than antidepressant medication alone.

NCT ID: NCT00174876 Completed - Depression Clinical Trials

Aripiprazole as Augmentation for TRD

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

A sizeable minority of patients suffering from major depression do not have their full set of depressive symptoms relieved by a single medication. Often times, a second medication is added to a patient's first antidepressant to obtain a better response in hopes of getting the depressed patient into full remission from symptoms. A typical psychiatric approach of recent has been to add one of the newer anti-schizophrenia medications to an existing FDA approved antidepressant in order to achieve better serotonin levels in the depressed patient's brain. This optimization of brain serotonin helps to alleviate more depressive symptoms. The newest antipsychotic medication to be FDA approved is Aripiprazole (Abilify). It may be particularly effective as it may safely elevate sertotonin through receptor 1a stimulation, receptor 2a blockade. It may also facilitate low levels of dopamine transmission which is truly novel for this agent when compared to other schizophrenia drugs. Depressed patients also tend to lack dopamine in their brains. This makes Aripiprazole and ideal agent to boost both serotonin and dopamine simultaneously. In theory, this may be an effective way to alleviate more depressive symptoms. The author suggests to enroll 10 subjects initially in open label fashion to take Aripiprazole plus their current FDA approved antidepressant to see if further elimination of depressive symptoms occurs and to show this pharmacological approach as a tolerable combination of medications. If there are no major safety issues, an amendment to allow 10 additional subjects will be forwarded to provide a better tolerability sample size.

NCT ID: NCT00172848 Completed - Depression Clinical Trials

Mastery, Social Support and Depression of Patients With Major Depression

Start date: October 2004
Phase: Phase 1
Study type: Observational

The purpose of this study was to discuss the relation of mastery, social support and depression in patients with depressive disorder. Cross-sectional quantitive study and purposive sampling method were designed. Data collection and analysis was conducted through structural questionnaires (including demographics, social support scale, mastery scale, CESD scale) at a medical center in Taipei. Results showed that patients with depression whose degree of depression was negative correlated with mastery and social support, and mastery was positive correlated with social support. Regression statistics results showed that mastery, social support, age, loss of jobs can predict degree of depression up to 60 percent. The mastery was strongest independent predictable factor to degree of depression, and had partial or total mediate effects to age, loss of jobs, financial condition, and social support. The result of this study suggested that clinically the care of patients with depression should focus on their confidence in mastery and provide strategies to promote their confidence in mastery, which can effectively reduce the degree of depression of those patients.