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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT01204086 Recruiting - Clinical trials for Major Depressive Disorder

Pharmacogenomics Studies of Antidepressants

Start date: March 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to establish the clinical effectiveness of antidepressants by pharmacogenomic approach, and to determine the levels of inflammatory factors between the baseline and the end point of the study in Taiwanese major depressive disorder (MDD) patients.

NCT ID: NCT01198561 Recruiting - Clinical trials for Major Depressive Disorder

Repetitive Transcranial Magnetic Stimulation(rTMS) in the Treatment of Depression

Start date: February 2006
Phase: N/A
Study type: Observational

The objective of this study is to investigate the antidepressant efficacy of rTMS, and to assess cortical metabolism before and after rTMS sessions in patients with major depression. We also aimed to investigate differences between the responders and nonresponders to rTMS and what would predict clinical response to rTMS.

NCT ID: NCT01170520 Recruiting - Clinical trials for Adolescent Depression

Repetitive Transcranial Stimulation (rTMS) for Resistant Depression in Adolescents

Start date: August 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators hypothesis that repetitive transcranial Stimulation (rTMS) is a safe and effective add-on therapy for resistent depression in adolescent patients. A group of adolescents suffering from non psychotic major depression that was resistant to at least 2 drug trials and a trail of psychotherapy will be recruited. After an informed consent procedure for both parents and patients, patients will go through a clinical and cognitive evaluation. They will receive a protocol of 4 weeks (20 work days) of rTMS using the figure of 8 magstim coil at 100% threshold, 42 trains of 4 seconds each, intertrain interval of 30 sec to the LDPC, 1680 pulses per day. Then they will be reevaluated.

NCT ID: NCT01070134 Recruiting - Clinical trials for Major Depressive Disorder

Mindfulness-based Behavioural Therapy (MIBT) Versus Psychodynamic Therapy for Patients With Major Depressive Disorder in Psychotherapeutic Day Treatment. A Randomised Clinical Pilot Trial

Mipsy
Start date: February 2010
Phase: N/A
Study type: Interventional

Background: According to the WHO, major depressive disorder is the second largest healthcare problem worldwide in terms of disability caused by illness. It afflicts an estimated 17% of individuals during their lifetimes at tremendous costs. A number of depressive patients are treated with antidepressant medication. The efficacy of antidepressant medication has been studied in a number of systematic reviews, and in recent years some of these reviews have shown that the efficacy is questionable for many patients. So are there other effective treatments for this serious illness? Cognitive- and psychodynamic therapies are probably both significantly more effective for depression than no treatment, but only limited comparisons have been made between the two interventions. A Cochrane review shows that cognitive therapy has a preventive effect against recurrent depression, and that this effect may surpass the preventive effect of antidepressant medication. Mindfulness training may be an effective technique in preventing relapse in patients who have had at least 3 previous depressive episodes. But efficacy in treating currently depressed patients has not been studied. Objective To perform a randomised clinical trial with blinded assessment of efficacy variables in order to study the effects of mindfulness based behavioral therapy (cognitive therapy and mindfulness) versus psychodynamic therapy in depressive patients. Methods A randomised clinical trial of 84 consecutive patients diagnosed with major depressive disorder, referred to the day clinic, Roskilde psychiatric services. The patients will be randomised to one of two interventions: 1. MIBT (mindfulness-based behavioural therapy) 2. PT (psychodynamic therapy)

NCT ID: NCT01062880 Recruiting - Major Depression Clinical Trials

Neuropattern - Assessment of a Translational Diagnostic Tool for Depression, Adjustment- and Somatoform-disorders

Neuropattern
Start date: February 2010
Phase: N/A
Study type: Interventional

Neuropattern is a first translational tool in stress medicine. Neuropattern is a diagnostic tool, which can be applied by in- and outpatients and physicians to detect dysregulation in the stress response network. The physician provides anamnestic and anthropometric data, while the patient takes other measures at home, e.g. psychological, symptomatic, and biological data. Among the biological data are ECG measures for analyses of heart rate variability, and salivary cortisol measures before and after a dexamethasone challenge test. All data are analyzed in a central laboratory, which generates a written report for the physician, including a disease model, from which personalized recommendations for pharmacological and psychological treatments are derived. Neuropattern additionally offers individualized internet modules to inform the patient about the disease model and to teach him/her what he/she can do to improve his/her medical conditions. The current study applies Neuropattern in 2000 patients of family doctors, suffering from major depression, depressive episodes, adjustment disorders, and somatoform disorders. The patients receive either unspecific or individualized internet modules in a randomized order.

NCT ID: NCT01047124 Recruiting - Clinical trials for Chronic Unipolar Depressive Disorder

Trial of the Clinical and Cost Effectiveness of a Specialist Expert Mood Disorder Team for Refractory Unipolar Depressive Disorder

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is determine whether a specialised mood disorder service, which offers tailored psychological and pharmacological treatment, is more effective in the treatment of chronic unipolar depressive disorder then treatment as usual.

NCT ID: NCT00984685 Recruiting - Depression Clinical Trials

"Assessment of Risk Factors for Depression Treatment at a Safety Net Clinic"

Start date: August 2009
Phase: N/A
Study type: Observational

The purpose of the study is to identify the barriers for effective treatment of depression, specifically whether modified CHIS Scale is a valid tool for identifying the high risk patients for depression.

NCT ID: NCT00927550 Recruiting - Depression Clinical Trials

Lithium and Standard Therapy in Resistant Depression

LAST
Start date: June 2009
Phase: Phase 4
Study type: Interventional

The principal clinical question is whether lithium is effective in reducing the risk of suicidal behaviour in subjects with treatment-resistant depression and suicide risk. Additionally aims of the study are: (a) to assess whether lithium is effective in improving depressive symptomatology in subjects with treatment-resistant depression and suicide risk; (b) to assess the tolerability profile of lithium.

NCT ID: NCT00896090 Recruiting - Depression Clinical Trials

Cortical Excitability and Inhibition in Children and Adolescents With Major Depressive Disorder

Start date: April 2009
Phase: Phase 1
Study type: Observational

This study is being done to determine whether measures of brain activity (known as cortical excitability and inhibition) collected by Transcranial Magnetic Stimulation (TMS) are different in children and adolescents with depression and children and adolescents that do not have depression.

NCT ID: NCT00889369 Recruiting - Clinical trials for Major Depressive Disorder

Duloxetine for Major Depression in Peri-/Postmenopausal Women

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

The main objective of this study is to characterize a range of brain activation symptoms associated with major depression in peri- and post-menopausal women. Also, assessing brain activation before and after the treatment might help to uncover some mechanisms associated with the pathophysiology of depression and menopause.