Clinical Trials Logo

Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

Filter by:

NCT ID: NCT00970437 Completed - Clinical trials for Chronic Major Depressive Disorder

A Comparison of Cognitive Behavioral Analysis System of Psychotherapy (CBASP) and System of Supportive Psychotherapy (SYSP) for Early Onset Chronic Depression

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of the Cognitive Behavioural Analysis System of Psychotherapy (CBASP) with the non-specific System of Supportive Psychotherapy (SYSP)in early onset chronically depressives.

NCT ID: NCT00969709 Completed - Clinical trials for Major Depressive Disorder

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety, and tolerability of Levomilnacipran ER fixed doses versus placebo in the treatment of outpatients with major depressive disorder.

NCT ID: NCT00969150 Completed - Clinical trials for Major Depressive Disorder

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety, and tolerability of Levomilnacipran ER versus placebo in the treatment of outpatients with major depressive disorder.

NCT ID: NCT00965497 Completed - Multiple Sclerosis Clinical Trials

Escitalopram (Lexapro) for Depression MS or ALS

Start date: July 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if escitalopram (Lexapro) improves symptoms of major depressive disorder in patients who have ALS or MS.

NCT ID: NCT00964054 Completed - Unipolar Depression Clinical Trials

Depression Outcomes Study of Exercise

DOSE
Start date: September 2012
Phase: Phase 1
Study type: Interventional

This pilot study may yield important research findings on how to adapt exercise treatment for depression among adolescents. Potential public health benefits from this study include a reduction of adolescent depression and problems associated with untreated depression in young adults including suicide, substance abuse, cigarette smoking, teen pregnancy, impaired psychosocial functioning and school failure. In addition, because this study prescribes physical activity as a treatment for depression, additional public health benefits may include a reduction in chronic diseases such as obesity, diabetes and heart disease, all of which are associated with sedentary behavior.

NCT ID: NCT00962598 Completed - Clinical trials for Depressive Disorder, Major

The Role Of Omega-3 Fatty Acids In Adolescent Depression

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

The purpose of this study is to examine the effects of a 10-week Omega-3 Fatty Acid treatment phase on brain chemistry of adolescents with major depressive disorder (MDD) using proton magnetic resonance imaging.

NCT ID: NCT00961454 Completed - Clinical trials for Post-Traumatic Stress Disorder

Photobiomodulation to Alter Cerebral Blood Flow and to Affect the Emotional Status of Patients With Major Depression

Start date: January 2009
Phase: Phase 1
Study type: Interventional

A pilot study to evaluate the ability of photobiomodulation to alter cerebral blood flow in the frontal poles and to affect the emotional status of patients with major depression.

NCT ID: NCT00961402 Completed - Clinical trials for PostPartum Depression

The Effect of Exercise on Preventing PostPartum Depression

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the feasibility and efficacy of an exercise intervention for the prevention of postpartum depression. If efficacious, our intervention could be disseminated in "real world settings" in an effort to prevent postpartum depression.

NCT ID: NCT00960986 Completed - Clinical trials for Major Depressive Disorder (MDD)

A Duloxetine Dosing Strategy Study in Korean Patients With Major Depressive Disorder

Start date: August 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess nausea severity in response to four different drug dosing strategies of Duloxetine (30 mg with food, 60 mg with food, 30 mg without food, and 60 mg without food) in Korean patients with major depressive disorder (MDD).

NCT ID: NCT00960830 Completed - Depression Clinical Trials

Mirtazapine Reduces ICD Shocks in ICD Patients With Depression and Anxiety

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if the use of antidepressant medication in depressed patients with implantable cardioverter defibrillator reduces the number of ICD's shocks as it improves depressive affect.