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Depressive Disorder, Major clinical trials

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NCT ID: NCT00227812 Completed - Clinical trials for Depressive Disorder, Major

Integrated Treatment for Cocaine and Mood Disorders - 1

Start date: April 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test whether cognitive behavioral therapy and bupropion hydrochloride will help cocaine users, who are depressed, reduce or end their cocaine use and improve their mood.

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: NCT00223288 Completed - Asthma Clinical Trials

Impact of Caregiver Depression on Asthma in the Child

Start date: March 2003
Phase: Phase 4
Study type: Observational

This study will examine if depression in a primary caregiver is associated with more hospitalization or ER visits in children with asthma. This study will also explore whether treatment for depression in the primary caregivers is associated with improvement in asthma in school-aged children. Asthma is a very common childhood disorder of airway inflammation. The causes include environmental irritants, cold temperature, and infection in the respiratory tract, and emotional factors can contribute to symptom exacerbation. However, asthma is a disease that can be well controlled if there is proper medication compliance and careful control of environmental conditions. Data suggests that psychiatric symptoms in the mothers of children with asthma are associated with more asthma related hospitalizations in children. Thus, we want to explore this question further using more specific diagnostic instruments in order to detect what types of symptoms are associated with increased asthma related service utilization. Also, we want to explore if effective treatment of the caregivers' symptoms is associated with decreased hospitalization and emergency room visits for the child.

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: NCT00222820 Completed - Major Depression Clinical Trials

Depression: The Search for Treatment-Relevant Phenotypes-Pilot Study

Start date: April 2002
Phase: Phase 4
Study type: Interventional

We are doing this pilot study to learn more about four aspects of treating depression: 1. The features of a depressed person’s mood and anxiety and how these features affect a person’s capacity to get better and stay better. 2. If depressed people with certain features of mood and anxiety respond better to therapy, medication or a combination of therapy and medication. 3. Whether or not a person’s personality traits affect how they respond to treatment. 4. The gene involved in processing antidepressant medication

NCT ID: NCT00220636 Completed - Clinical trials for Depressive Disorder, Major

Abilify as an Adjunctive Treatment for Refractory Depression

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

This is a study of the effectiveness of adding Abilify (aripiprazole), an atypical antipsychotic medication, to ongoing selective serotonin reuptake inhibitor (SSRI) antidepressant treatment for depressed outpatients who are not responding fully to SSRI treatment alone. It is hypothesized that patients' functioning will improve after 12 weeks of treatment with Aripiprazole and SSRI medication.

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: 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: 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.