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Depression clinical trials

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NCT ID: NCT00532376 Withdrawn - Depression Clinical Trials

fMRI Investigation of Depression in Patients With Epilepsy

Start date: September 2005
Phase: N/A
Study type: Observational

Depression is very common in epilepsy. Depression is the strongest predictor of poor quality of life in patients with epilepsy. The biological basis for depression in epilepsy remains poorly understood. This study uses functional MRI (fMRI) to examine brain response to emotional and non-emotional stimuli in healthy control subjects and in patients with epilepsy who are either depressed or not depressed. Results from this study will contribute to a better understanding of depression in epilepsy, which may eventually inform development of better treatment modalities..

NCT ID: NCT00525928 Withdrawn - Smoking Clinical Trials

Mood and Anti-craving Effects of Varenicline in Psychiatric Inpatients

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

This study of psychiatric inpatients will assess mood effects of varenicline, as well as assess if varenicline decreased nicotine cravings acutely. This study will also measure side effects of varenicline when given in addition to other psychiatric and non-psychiatric medications.

NCT ID: NCT00517972 Withdrawn - Depression Clinical Trials

Omacor for Perimenopausal Depression

Start date: n/a
Phase: Phase 2
Study type: Interventional

Recently, antidepressants and other similar acting agents have been explored as a class of medications to treat major depressive disorder (MDD) in the context of perimenopause, as well as the somatic symptoms of perimenopause (such as hot flashes). Omega-3 fatty acids, which include eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are nutritional compounds with widely established health benefits and which occur naturally in fish and marine sources. Results of previous mood disorder studies have indicated that omega-3 fatty acids may be of help in the treatment of depression. Therefore, the current study is designed to examine the effectiveness and tolerability of the study drug, Omacor, (omega-3 fatty acid ethyl esters), in the treatment of major depressive disorder in perimenopausal women.

NCT ID: NCT00470639 Withdrawn - Bipolar Depression Clinical Trials

Transcranial Magnetic Stimulation for Bipolar Depression

Start date: April 2007
Phase: Phase 1/Phase 2
Study type: Interventional

This is a study to assess the effectiveness of repetitive transcranial magnetic stimulation (rTMS) as a treatment for depressed adults with bipolar disorder. In rTMS high-intensity, fluctuating magnetic fields non-invasively stimulate the cortex of the brain depolarising neurons. No anaesthetic is required and the treatment in subconvulsive. Recent studies suggest that rTMS can be an effective treatment for depressive illness in adults (Loo and Mitchell et al, 2005) and appears to be quite safe. Most of the published studies to date have focused on unipolar depression. There is limited data of TMS use in bipolar depression. Eg. Pilot study by Nahas Z, Kozel FA, Li X, Anderson B, George MS.in 2003, which was negative. The investigators wish to assess this in a sham-controlled study of adults. The investigators hypothesise that both left and right sided rTMS will have an antidepressant effect superior to sham in this population.

NCT ID: NCT00460200 Withdrawn - Depression Clinical Trials

Depression and Interleukin-6 Production in Patients With Ovarian Epithelial Cancer

Start date: December 2003
Phase: N/A
Study type: Observational

RATIONALE: Measuring levels of interleukin-6 and depression may help doctors understand the relationship between interleukin-6 and depression. It may also help the study of cancer in the future. PURPOSE: This clinical trial is studying depression and interleukin-6 production in patients with ovarian epithelial cancer.

NCT ID: NCT00451490 Withdrawn - Clinical trials for Depressive Disorder, Major

The Effect of Agomelatine or Fluoxentine on Heart Rate Variability in Patients With Major Depressive Disorder

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

Phase advance of HRV will be anticipated in agomelatine group. It is anticipated that both agomelatine and floxentine will increase HRV at the end of the treatment.

NCT ID: NCT00429689 Withdrawn - Depression Clinical Trials

Hormonal Levels in Men With Major Depressive Disorder

Start date: n/a
Phase: N/A
Study type: Observational

Subjects will be 1000 men meeting the following inclusion criteria: 1) male, age 18-65 years; 2) meeting DSM-IV criteria for major depressive disorder within the past one year, with a HAM-D score >12. Subjects will be excluded if they exhibit 1) a substance abuse or dependence disorder within the past year; 2) current psychotic symptoms; or 3) a history of bipolar disorder. Procedure After informed consent, eligible patients will have blood drawn for serum hormone levels; cortisol, DHEA-S and testosterone or they will provide a salivary sample for measurement of hormone levels. We will also test hormone level form 1000 healthy males (from blood or saliva) at the same age for comparison.

NCT ID: NCT00386893 Withdrawn - Depression Clinical Trials

Somatosensory Processing in Depression

Start date: October 2006
Phase: Phase 4
Study type: Interventional

Aim of this study is to investigate neuronal differences (EEG/evoked potentials; functional MRI) between patients with major depression and healthy controls concerning brain activity after acute pain as well as changes of pain related brain activity during treatment with escitalopram.

NCT ID: NCT00359125 Withdrawn - Bipolar Depression Clinical Trials

RU-486 in the Treatment of Bipolar Depression

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

Bipolar disorder is a chronic and recurrent illness which involves episodes of mania and depression. It is believed that disturbance of the stress hormone system (the hypothalamic-pituitary-adrenal or HPA axis) may cause thinking and memory problems and make the depressive symptoms worse in bipolar disorder. Early studies have shown that mifepristone may have antidepressant effects (may improve the symptoms of depression) and may also maintain or enhance cognition (memory and thinking functions). The purpose of this study is to determine the potential therapeutic efficacy (usefulness) of mifepristone in bipolar depression by assessing the effects of the medication on depressive symptoms and on cognition. This will be done by questionnaires and thinking tests. This study will also try to clarify the functional changes that accompany bipolar disorder by analyzing saliva samples (assessing the stress response by measuring the levels of 2 stress hormones: cortisol and DHEA).

NCT ID: NCT00338273 Withdrawn - Bipolar Disorder Clinical Trials

A Study of Aripiprazole in Patients With Bipolar I Disorder With a Major Depressive Episode

Start date: December 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate flexible doses (5-30 mg) of aripiprazole in patients with bipolar depression.