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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT00218556 Completed - Hepatitis C Clinical Trials

Preventing Depression in Methadone Maintenance Patients Receiving Hepatitis C Treatment - 1

Start date: January 2004
Phase: N/A
Study type: Interventional

The purpose of this study is develop and test a cognitive-behavioral intervention to prevent depression in methadone maintenance patients receiving medical treatment for hepatitis C.

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: NCT00215176 Completed - Atypical Depression Clinical Trials

Modafinil for Atypical Depression

Start date: February 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The purposes of the study are to: 1) evaluate the short-term efficacy and safety of modafinil in atypical depression; and 2) to evaluate the efficacy of modafinil in preventing relapse of atypical depression. The hypothesis is that modafinil is safe and effective in the treatment of atypical depression.

NCT ID: NCT00214682 Completed - Depression Clinical Trials

Beyond Ageing Project: A Study for the Prevention of Depression

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

The purpose of this study is to determine whether folate and vitamin B12, physical activity and mental health literacy can prevent depression, and folate and vitamin B12 and physical activity can prevent cognitive impairment in older people. Also the study aims to assess the benefits for older people in improving their knowledge about mental health in relation to depression.

NCT ID: NCT00212797 Completed - Depression Clinical Trials

A Study to Determine the Efficacy and Safety of 2 Doses of Org 34517 as Adjunctive Therapy in Subjects With Psychotic Major Depression (28130)(P05845)

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

The primary purpose of this study is to determine whether subjects with psychotic major depression benefit from adjunctive treatment with Org 34517. Two doses of Org 34517 will be compared to placebo in this international multicenter study. The duration of this trial is 6 weeks.

NCT ID: NCT00211835 Completed - Depression Clinical Trials

Treatment of Post-TBI Depression

Start date: November 2005
Phase: N/A
Study type: Interventional

Randomized clinical trial that compares the effects of cognitive behavioral therapy (CBT) and supportive psychotherapy for depression. Short- and long-term outcomes will be evaluated in terms of changes in mood (primarily depression and anxiety), participation in activities and life satisfaction.

NCT ID: NCT00209170 Completed - Depression Clinical Trials

Depression-Diabetes Mechanisms: Urban African Americans

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

African-Americans suffer from increased prevalence of both type 2 diabetes and diabetes complications, reflecting a combination of psychobehavioral factors as well as metabolic dysfunction. In this process, depression may contribute to both the genesis of type 2 diabetes (through impact on neurohormonal activation, inflammatory mediators, and insulin resistance), and difficulties in management (through decreased adherence to diet plans, medication, and scheduled appointments). The preliminary data from the Grady Diabetes Clinic indicates that depression may be common in African-Americans with diabetes, that depression is a factor in non-adherence, and that non-adherence leads to poor glycemic control - a direct cause of diabetes complications. What is not known is: how treatment of depression could lead to both neurohormonal and psychobiological improvement, with improved patient adherence and glycemic control.

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.