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Major Depressive Disorder clinical trials

View clinical trials related to Major Depressive Disorder.

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NCT ID: NCT00229398 Completed - Clinical trials for Major Depressive Disorder

Medical and Psychiatric Co-Morbidity Among Treatment Resistant Patients With Major Depression Disorder

Start date: November 1998
Phase: N/A
Study type: Observational

Assessing psychiatric and physiological co-morbidity in TRD and non-TRD patients

NCT ID: NCT00229294 Completed - Clinical trials for Major Depressive Disorder

Fibromyalgia in Men Suffering From PTSD

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

Assessing FM and psychiatric state among PTSD, MDD and healthy participants

NCT ID: NCT00226278 Completed - Clinical trials for Major Depressive Disorder

Safety Study of ORG 34517 for Major Depression With Psychotic Features

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

Patients suffering from Major Depressive Disorder with Psychotic features who have received no changes in their medications in the previous two weeks will receive "usual" treatment of antidepressants, antipsychotics and/or mood stabilizers and adjunct therapy using ORG34517. The patient will be hospitalized for up to two weeks to monitor their medications and progress and will return to the site for periodic assessments.

NCT ID: NCT00223197 Completed - Clinical trials for Major Depressive Disorder

Pregnenolone Trial for Depression in Bipolar Disorders or Recurrent Major Depressive Disorder With Substance Abuse

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

The purpose of this research is to determine if pregnenolone supplement is associated with a reduction in substance use and craving in patients with recurrent major depressive disorder or bipolar disorder and substance abuse/dependence. This research also wants to explore if pregnenolone supplements are associated with improvement in psychiatric symptoms and memory, which are often negatively affected in these patients. It is hypothesized that patients receiving pregnenolone supplements would show greater improvements in mood symptoms and memory, and crave substances less than the patients receiving placebo.

NCT ID: NCT00215228 Completed - Clinical trials for Major Depressive Disorder

Effects of Duloxetine vs. Escitalopram on Heart Rate Variability in Depression

Start date: July 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Low heart rate variability is a marker of increased risk of cardiac mortality, and is observed in depressed coronary artery disease patients. Some antidepressants may themselves, however, decrease heart rate variability. We will test the hypothesis that greater reduction in heart rate variability will be associated with duloxetine (which has noradrenergic activity) than escitalopram (a selective serotonin reuptake inhibitor). We will also test the hypothesis that changes in heart rate variability are related to the magnitude of norepinephrine transporter occupancy.

NCT ID: NCT00209105 Completed - Clinical trials for Major Depressive Disorder

Characterizing Psychological Consequences of Childhood Trauma

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

This study will characterize the mental health consequences of early-life trauma.

NCT ID: NCT00209066 Completed - Clinical trials for Major Depressive Disorder

Treatment of Reduced Heart Rate Variability Associated With Major Depression With Electroconvulsive Therapy

Start date: November 1998
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate alterations in sympathetic tone in patients with major depression with and without ischemic heart disease and then to reevaluate these patients after 8 treatments with electroconvulsive therapy(ECT). We expect to support the hypothesis that HRV are pathophysiologically associated with the state of major depression. We hypothesize the following: 1. Heart rate variability (HRV) will be decreased prior to treatment of depression in comparison to post-treatment measures of HRV. 2. After 8 treatments with ECT, HRV will be increased under basal conditions.

NCT ID: NCT00208897 Completed - Clinical trials for Major Depressive Disorder

Does Fluoxetine Have an Effect on the CNS CRF Systems in Women Abused in Childhood?

Start date: December 1997
Phase: N/A
Study type: Interventional

The primary objective of this project is to determine whether treatment with the SSRI, fluoxetine versus placebo reverses alterations in the central CRF system induced by early life stress experiences (i.e. childhood sexual and/or physical abuse) in cases with and without major depression. We also evaluate whether neuroendocrine changes after SSRI treatment correlate with clinical improvement.

NCT ID: NCT00208169 Completed - Schizophrenia Clinical Trials

Abilify Therapy for Reducing Comorbid Substance Abuse

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

It is hypothesized that the use of aripiprazole (Abilify) in patients with alcohol and/or drug dependence with comorbid psychiatric conditions will lead to: - Reduction in the amount of alcohol and/or drugs used as measured by the Time Line Follow Back (TLFB) and the Addiction Severity Index (ASI) - Reduction in cravings for alcohol and drugs as measured by the Penn Alcohol Craving Scale - Reduction in symptoms of co-morbid psychiatric disorders compared to before starting aripiprazole.

NCT ID: NCT00205946 Completed - Clinical trials for Major Depressive Disorder

The Effects of Acute Administration of Bupropion on Neural Substrates Underlying Hedonic Capacity

Start date: April 2005
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the effects of a single-dose of Wellbutrin XL (bupropion hydrochloride) on reward processing.