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Active clinical trials for "Depressive Disorder, Major"

Results 971-980 of 2240

A Study of Adjunctive Aripiprazole in Patients With Major Depressive Disorder

Major Depressive Disorder

This trial is a 14 week, randomized, double-blind, placebo controlled study, to assess the safety and efficacy of aripiprazole as adjunctive treatment to an ongoing antidepressant treatment in patients with Major Depressive Disorder.

Completed3 enrollment criteria

An 8 Week Study Of Depression In Adults Diagnosed With Major Depressive Disorder

Depressive DisorderMajor

A Placebo Controlled Study Evaluating Efficacy, Safety and Tolerability of Medication in Patients with Major Depressive Disorder (MDD)

Completed10 enrollment criteria

Effects of Antidepressants on Sexual Functioning

Major Depressive Disorder (MDD)

The purpose of this trial is to study the effects of two depression medications on sexual functioning.

Completed7 enrollment criteria

Effects Of Antidepressants On Sexual Functioning In Adults

Major Depressive Disorder (MDD)

This study will evaluate the effects of two antidepression medications on sexual functioning.

Completed7 enrollment criteria

Major Depressive Disorder Study In Adults

Major Depressive Disorder

A study to obtain safety and tolerability data

Completed10 enrollment criteria

Fixed Dose Comparison of Escitalopram to an Active Comparator in Severely Depressed Patients

Major Depressive Disorder

The purpose of this study is to evaluate the safety and efficacy of escitalopram to an active comparator in severely depressed patients

Completed8 enrollment criteria

Study Of Bupropion SR (323U66) In Patients With Major Depressive Disorder In Japan

Major Depressive Disorder (MDD)

This is a study to obtain clinical experience of 323U66 SR for elderly patients with depression in repeat-dose of 323U66 SR up to 300mg/day, and to conduct exploratory investigation on safety, efficacy and pharmacokinetics profile in elderly patients with depression.

Completed32 enrollment criteria

Study Evaluating DVS-233 SR In Adult Outpatients With Major Depressive Disorder

Major Depressive Disorder

Primary Objective: To compare the antidepressant efficacy and safety of subjects receiving DVS-233 SR versus subjects receiving placebo. Secondary Objective: To assess the response of subjects receiving DVS-233 SR for the clinical global evaluation, functionality, general wellbeing, pain, and absence of symptoms (Hamilton Psychiatric Rating Scale for Depression, 17-item [HAM-D17] less than or equal to 7) versus those subjects receiving placebo.

Completed6 enrollment criteria

Combining Antidepressant Medication and Psychotherapy for Insomnia to Improve Depression Outcome...

Major Depressive DisorderInsomnia

This study will examine the effectiveness of a combination of antidepressant medication and sleep-focused psychotherapy to simultaneously treat sleep difficulties and depression.

Completed19 enrollment criteria

Hippocampal Volume in Young Patients With Major Depression Before and After Combined Antidepressive...

Depressive DisorderMajor

The proposed study is a randomized, placebo-controlled, double-blind trial to evaluate the safety and efficacy of antidepressant combination for the treatment of depression. Depressive disorder is one of the most common human diseases with a high burden for every patient, her/his family, health care system and society as a whole. Actual treatment concepts of depressive disorders include pharmacologic, biologic (e.g. electroconvulsive therapy, light therapy) and psychologic therapy. Even though effective therapeutic options are at hand, therapy needs time. It is often not possible to reach full remission of the disease and 10-25% of patients suffering from depression are regarded as "treatment-resistant". In treatment resistant depression, the use of a combination of antidepressive drugs is considered safe and effective. However, at present no data exist concerning the use of drug combination as primary therapeutic option. The aim of the study is to examine the hypothesis, that significantly more patients achieve full remission of depressive symptoms when treated with the combination of two antidepressants and as a secondary hypothesis, that patients receiving a drug combination will achieve remission faster than patients treated with monotherapy. To test these hypotheses, a two group parallel design is used comparing the efficacy and safety of mirtazapine in combination with venlafaxine or placebo.

Completed14 enrollment criteria
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