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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT00729755 Completed - Clinical trials for Major Depressive Disorder

Creatine Augmentation Treatment in Major Depressive Disorder Subjects

Start date: August 2008
Phase: N/A
Study type: Interventional

Given 1) the established safety with short-term or long-term supplementation of Cr, 2) its potential usefulness in improving brain energy metabolism, 3) the reported abnormality in brain energy metabolism in MDD subjects, and 4) plausible association between depression and inflammatory mediators, we hypothesize that oral Cr augmentation will help reduce symptoms in MDD patients as well as normalize a deficit in brain energy metabolism and that improvement of MDD and brain energy metabolism will be correlated with inflammatory mediators changes. In this study, we plan to conduct an randomized, double-blind, placebo-controlled augmentation study with creatine in addition to escitalopram. We will assess the efficacy and safety of the Cr augmentation and evaluate changes relevant to brain energy metabolism and inflammatory mediators.

NCT ID: NCT00729547 Completed - Depression Clinical Trials

The Therapeutic Efficacy of Neurofeedback in Depression

neurofeedback
Start date: September 2006
Phase: N/A
Study type: Interventional

The investigators examined the therapeutic efficacy of neurofeedback in depression subjects. The investigators hypothesize that 5 weeks neurofeedback training will be able to alleviate depressive symptoms.

NCT ID: NCT00728208 Completed - Depressive Disorder Clinical Trials

GSK372475 PK Study in Healthy Volunteers

Start date: July 28, 2008
Phase: Phase 1
Study type: Interventional

This study will consist of 4 parallel cohorts of healthy volunteers (elderly male, elderly female, young male and young female). Subjects will receive either GSK372475 1.5mg or placebo for 28 days.

NCT ID: NCT00723970 Completed - Clinical trials for Major Depressive Disorder

Quetiapine Extended Release (XR) for the Treatment of Menopausal Depression

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

The study was designed to examine the efficacy and tolerability of quetiapine XR for the treatment of women who suffer from depression in the context of the menopausal transition and postmenopausal years. Besides the improvement of depressive symptoms, the investigators are interested in examining the impact of this medication on vasomotor symptoms (hot flashes, night sweats), sleep and overall quality of life.

NCT ID: NCT00720473 Completed - Bipolar Depression Clinical Trials

Lamotrigine Therapy in Geriatric Bipolar Depression

Start date: April 2006
Phase: N/A
Study type: Interventional

We propose to study the efficacy and tolerability of lamotrigine in the treatment of older adults with bipolar depression and to compare measures of brain energy metabolism between older subjects with bipolar depression and healthy age-matched controls in order to better understand treatment response in geriatric bipolar depression.

NCT ID: NCT00720369 Completed - Bipolar Depression Clinical Trials

CoQ10 in Geriatric Bipolar Depression

CoQ10
Start date: July 2008
Phase: N/A
Study type: Interventional

We propose to study and compare measures of brain energy metabolism in geriatric bipolar individuals and healthy older adults. We would also like to investigate changes in brain energy metabolites and in vivo creatine kinase (CK) enzymatic activity associated with CoQ10 administration in older bipolar individuals.

NCT ID: NCT00719979 Completed - Depression Clinical Trials

Effectiveness of a Technology Assisted Behavioral Intervention in Assisting People With Major Depressive Disorder

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

This study will develop and evaluate the effectiveness of a technology-assisted behavioral intervention, consisting of Internet-based cognitive behavioral therapy combined with telephone and email support, in reducing depressive symptoms and improving treatment adherence in primary care patients with major depressive disorder.

NCT ID: NCT00719706 Completed - Bipolar Depression Clinical Trials

The Use of a Mitochondrial Enhancement Treatment in Bipolar Disorder

Start date: August 2008
Phase: Phase 2
Study type: Interventional

The primary objective of this 15-week clinical trial is to test the hypothesis that treatment with two proven mitochondrial enhancers, acetyl-L-carnitine (ALCAR) and α-lipoic acid (ALA), has significantly greater efficacy than placebo as an augmentation treatment in bipolar depressed patients who display an incomplete response to conventional treatments.

NCT ID: NCT00718432 Completed - Depression Clinical Trials

An Interventional Study of Geriatric Frailty, Osteoporosis, and Depression

Start date: April 2008
Phase: N/A
Study type: Interventional

Frailty, osteoporosis, and depression are three highly prevalent geriatric syndromes. Having these conditions are associated with adverse outcome in physical health, mental health, quality of life, and daily functioning. They are associated with higher mortality rates as well as increased health care cost. Risk factors, pathogenesis, clinical phenotypes, and interventions of these three geriatric syndromes are often related. Frailty is often defined as accumulations of multi-system deficiencies with increased vulnerability to multiple worse outcomes. Multifactorial, interdisciplinary integrated care models targeting frail older adults may have positive impacts on measurements associated with not only frailty, but also depression, or osteoporosis. The objective of this proposed study is to conduct a randomized control trial (RCT) to exam the effectiveness of integrated interventions on multiple outcomes among community-dwelling Taiwanese elders with high risks for frailty and/or osteoporosis, depression. We also plan to determine the differential effects of intervention between urban and rural area.

NCT ID: NCT00717041 Completed - Depression Clinical Trials

Epidemiology of Depression, Anxiety, and Cognitive Impairment

Start date: May 2008
Phase: N/A
Study type: Observational

Many older adults have undetected health problems and lack basic prevention measures. Failure to identify and treat these conditions can lead to unnecessary morbidity and mortality and a decreased quality of life. Traditional screening and intervention programs, usually based in primary care providers' offices, have been insufficient, particularly in medically underserved populations. Alternate sites for screening and intervention have begun to receive attention and may hold promise. The emergency department (ED) is the entry point for access to medical and social services for many patients and has the potential to serve as a site to identify older adults with unmet needs. However, we do not know the prevalence of depression and cognitive impairment and how they differ by mode of arrival of the patient to the ED. Second, a question remains as to the validity of screening patients during an acute illness. Upon completion, this study will describe the epidemiology of the population of older adults presenting to the ED.