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Major Depressive Disorder clinical trials

View clinical trials related to Major Depressive Disorder.

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NCT ID: NCT03062332 Recruiting - Clinical trials for Major Depressive Disorder

The Gut Microbiota of Bipolar and Depression

Start date: January 16, 2020
Phase:
Study type: Observational

Background: The gut microbiome is emerging as an important factor in regulating mental health yet it remains unclear what the target should be for psychiatric treatment. Investigators aim at elucidating the complement of the gut microbiome community for individuals with Major Depressive disorder (MDD) and Bipolar disorder (BD) relative to controls, and test for relationships with symptoms. Methods: Investigators prospect to recruit subjects including patients and controls amount to 240. All subjects will be collected for blood and stool samples,assessed by clinical scales. Finally, analyzing the correlation among the metabolon in blood, microbiota in stool and clinical scales to obtain the possible interaction between diseases and gut microbiota.

NCT ID: NCT03062267 Completed - Schizophrenia Clinical Trials

Effectiveness of a Mobile Texting Intervention for People With Serious Mental Illness

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Testing an mHealth mobile interventionist texting program on illness management.

NCT ID: NCT03053830 Completed - Clinical trials for Major Depressive Disorder

Open Label Ketamine Treatment for Major Depressive Disorder in Veterans

Ket-MDD
Start date: January 31, 2017
Phase: Phase 2
Study type: Interventional

Medically healthy Veterans ages 21-75 that have been diagnosed with Depression will get up to 6 treatments of Ketamine infusions, weekly. After treatment is completed, follow up will occur at 1 month, 3 months, and 6 months after completion of infusions to evaluate the longer term effects of ketamine.

NCT ID: NCT03053362 Completed - Clinical trials for Major Depressive Disorder

THINC-it Vortioxetine - Sensitivity to Change

Start date: May 24, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the sensitivity of the THINC-it tool, in measuring change in cognitive deficits in individuals with MDD after receiving vortioxetine.

NCT ID: NCT03051945 Withdrawn - Clinical trials for Major Depressive Disorder

Endogenous Opioid Modulation by Ketamine

Start date: August 2019
Phase: Phase 3
Study type: Interventional

Demonstrate the acute effects of ketamine on endogenous µ-opioid neurotransmission in humans.

NCT ID: NCT03051074 Completed - Clinical trials for Major Depressive Disorder

Examining the Effects of Reduced Environmental Stimulation on Anxiety

Start date: December 1, 2016
Phase: N/A
Study type: Interventional

The studies proposed in this protocol aim to explore the anxiolytic properties of floating as it relates to the central and autonomic nervous system.

NCT ID: NCT03031665 Completed - Clinical trials for Major Depressive Disorder

Sex, Hormones and Gamma-Aminobutyric Acid (GABA) in Stress Induced Anhedonia in Depression

Start date: October 1, 2017
Phase:
Study type: Observational

Using an innovative multi-modal imaging approach, this study investigates the role of the neurochemical gamma-aminobutyric acid (GABA), brain activity, as well as hormones in understanding sex differences in Major Depressive Disorder (MDD). Further, the investigators will link these markers to symptoms of depression.

NCT ID: NCT03026036 Completed - Clinical trials for Major Depressive Disorder

Neuroimaging Studies of Reward Processing in Depression

Start date: April 2016
Phase:
Study type: Observational

This study investigates stress-related signaling of glutamate and dopamine within the reward-processing circuit in Major Depressive Disorder (MDD), and whether they can be used to predict depressive symptoms in the future. This will be achieved through various neuroimaging tools (MRS, fMRI, PET), behavioral tasks, and a naturalistic follow-up design.

NCT ID: NCT03009448 Not yet recruiting - Clinical trials for MAjor Depressive Disorder

The Experience of Older Adults Facing Depression for the First Time in Old Age

Start date: March 2017
Phase: N/A
Study type: Observational

Analysis of recent studies show that researchers find it hard to distinguish between Late Onset Depression, a first diagnosed major depressive episode which occurs at old age, and Early Onset Depression, a depressive episode at old age with a history of previous episodes. Since current data, about the phenomenology and etiology of Late Onset Depression, lake conicity it is unclear whether this phenomena should be considered as a distinct subtype of depression. Nevertheless, the wide spread assumption is that Late Onset Depression has a stronger correlation with brain damage and environmental risk factors such as the common losses at old age and weaker correlation with family history and genetics when compared to Early Onset. Although many researchers consider brain damage to have the main contribution to the emerge of Late Onset Depression, the fact that depression has a negative effect on one's health supports the claim that it might be the result and not the rick factor. Since Late Onset Depression correlates with the common losses at old age, the investigators propose that an existential approach that deals with one's meaning, freedom, responsibly and death, might be more appropriate. Thus, the investigators ask how do older adults experience depression which they face for the first time in old age? Current study will seek to understand older adults' experience of Late Onset depression through existential paradigm by using a semi constructed interview.

NCT ID: NCT02999269 Completed - Clinical trials for Major Depressive Disorder

ECT Pulse Amplitude and Medial Temporal Lobe Engagement

Start date: October 2016
Phase: Phase 4
Study type: Interventional

Electroconvulsive therapy (ECT) remains the gold-standard treatment for patients with depressive episodes. During a typical four-week ECT series, most depressive episodes will respond to treatment and people will improve their level of functioning (return to work or family). Independent of the antidepressant effect of ECT, many patients experience transient memory impairment. This investigation will examine the impact of one ECT parameter (pulse amplitude or current) on brain changes (structure of connections within the brain) and clinical outcomes. The goal of this investigation is to determine the optimal parameter for an individual patient that will maintain the clinical response (reduce depression severity) and minimize side effects (eliminate memory issues related to treatment).