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Depressive Disorder clinical trials

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NCT ID: NCT00359125 Withdrawn - Bipolar Depression Clinical Trials

RU-486 in the Treatment of Bipolar Depression

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

Bipolar disorder is a chronic and recurrent illness which involves episodes of mania and depression. It is believed that disturbance of the stress hormone system (the hypothalamic-pituitary-adrenal or HPA axis) may cause thinking and memory problems and make the depressive symptoms worse in bipolar disorder. Early studies have shown that mifepristone may have antidepressant effects (may improve the symptoms of depression) and may also maintain or enhance cognition (memory and thinking functions). The purpose of this study is to determine the potential therapeutic efficacy (usefulness) of mifepristone in bipolar depression by assessing the effects of the medication on depressive symptoms and on cognition. This will be done by questionnaires and thinking tests. This study will also try to clarify the functional changes that accompany bipolar disorder by analyzing saliva samples (assessing the stress response by measuring the levels of 2 stress hormones: cortisol and DHEA).

NCT ID: NCT00294944 Withdrawn - Clinical trials for Major Depressive Disorder

The Effectiveness of Idazoxan in Treating TRD

Start date: n/a
Phase: Phase 3
Study type: Interventional

Assessing the effectiveness of Idazoxan as a treatment for depressive patients who did not respond to treatment with SSRI

NCT ID: NCT00276978 Withdrawn - Clinical trials for Therapy-resistant Depression

Aripiprazole Augmentation Therapy in Treatment-resistant Depression

Start date: June 2005
Phase: Phase 3
Study type: Interventional

20 therapy-refractory patients with major depression will be treated for 3 weeks with Aripiprazole 10 mg/d. Effectivity will be assessed using a pre-post comparison of different psychopathological rating scales and patient adherence.

NCT ID: NCT00273624 Withdrawn - Clinical trials for Therapy-resistant Depression

Olanzapine Augmentation Therapy in Treatment-resistant Depression: a Double-blind Placebo-controlled Trial

Start date: June 2005
Phase: Phase 3
Study type: Interventional

60 patients with major depression will be treated with 10 mg Olanzapine or Placebo for 2 weeks. In case of response (reduction of depressive symptoms)the study will be continued for further 60 days.

NCT ID: NCT00262665 Withdrawn - Clinical trials for Major Depressive Disorder

Randomized, Placebo-controlled Trial of an AMPAkine in Major Depressive Disorder

Start date: March 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test a candidate drug, Org 24448,in a phase II clinical trial in adult patients with moderately treatment-resistant unipolar major depressive disorder.

NCT ID: NCT00221494 Withdrawn - Depression Clinical Trials

Can Additional Drug Therapy Accelerate Response Time to Antidepressants

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

Antidepressants are commonly prescribed and are effective for treating depression. However, they generally take 4-6 weeks for a therapeutic response. This study is evaluating whether simultaneous treatment with thyroid hormone or pindolol can decrease the response time ("getting better faster") in patients who are starting SSRI treatment.

NCT ID: NCT00204503 Withdrawn - Clinical trials for Bipolar I or II Depression and Alcohol Abuse or Dependence

Open-Label Depakote ER in Patients With Bipolar I or II Depression and Alcohol Abuse or Dependence

Start date: June 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if Divalproex Sodium can be used to Treat and Prevent Depression in Patients with Bipolar Disorder who have Comorbid Alcohol Dependence/Abuse.

NCT ID: NCT00119028 Withdrawn - Clinical trials for Post-Traumatic Stress Disorder

Expanding and Testing VA Collaborative Care Models for Depression

ReTIDES
Start date: April 2005
Phase: N/A
Study type: Interventional

Based on the published evidence, collaborative care for depression is both necessary and sufficient for improving care and outcomes for depressed patients in primary care settings. The Translating Initiatives in Depression into Effective Solutions (TIDES) project, upon which ReTIDES is based, developed a VA-adapted version of collaborative care through input from veterans, clinicians, and managers. The initial TIDES project resulted in a clinically stable and effective model as tested in seven primary care practices in three VISNs. This positive result provided the basis for spreading and sustaining the TIDES model and initiating the study of national implementation strategies and issues.