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NCT ID: NCT01482221 Completed - Clinical trials for Major Depressive Disorder

A Study to Assess the Effect and Safety of AZD6765 in Patients With Major Depressive Disorder

Start date: December 16, 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effect and safety of AZD6765 in patients with major depressive disorder who exhibit inadequate response to antidepressants. AZD6765 is a channel blocker of the N-methyl-D-aspartate (NMDA) class of glutamate receptors.

NCT ID: NCT01477281 Not yet recruiting - Clinical trials for Chronic Venous Insufficiency

Study to Evaluate the Efficacy and Tolerability of Venaflon Use in Reducing the Symptoms Caused by Chronic Venous Insufficiency When Compared With Daflon

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The objective is to evaluate the effectiveness of the safety of Daflon in decreasing symptoms resulting from chronic venous insufficiency when compared with Daflon.

NCT ID: NCT01477203 Completed - Anxiety Disorder Clinical Trials

Multimodal Assessment of Neurobiological Markers for Psychiatric Disorders

MAN-BIOPSY
Start date: November 2011
Phase: Phase 4
Study type: Interventional

MAN-BIOPSY pursues the concrete research question whether novel biological and psycho-physiological clusters or categories can be defined to improve treatment and minimize side effects in psychiatry, based on a synopsis of physiological, behavioural, genetic and endocrinological parameters. One major aspect of our research approach is its focuses on the identification of dysfunctions in fundamental information processing mechanisms and neurocomputational mechanisms, and is not restricted to symptom-oriented tasks. The main objectives of MAN-BIOPSY are therefore - to identify biological and psycho-physiological parameters for major depressive disorders and anxiety disorders, and - to identify predictive markers for treatment response and type/severity of side effects for these disorders.

NCT ID: NCT01476865 Completed - Clinical trials for Arthritis, Rheumatoid

Articular Sonography: Healthy Subjects Versus Rheumatoid Arthritis Patients

Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to establish the normality of sonographic synovial measures in joints more affected in rheumatoid arthritis patients and establish, in those joints, a sonographic value of synovium predictive of rheumatoid arthritis.

NCT ID: NCT01476774 Completed - Clinical trials for Disease (or Disorder); Intervertebral Disc, With Myelopathy (Manifestation)

NORSPAN Transdermal Patches Phase III Study In Non-Cancer Pain

Start date: August 2009
Phase: Phase 3
Study type: Interventional

This is a multiple-dose, double-blind, double-dummy, active-control, parallel-group, multi-center, safety and efficacy study.

NCT ID: NCT01476527 Completed - Bipolar Disorder Clinical Trials

Deep Brain Stimulation for the Treatment of Refractory Bipolar Disorder

Start date: May 2011
Phase: N/A
Study type: Interventional

Bipolar Disorder (BD) is among the most comon and challenging conditions in psychiatry. Although episodes of mania and hypomania define the different types of the disorder, the clinical picture is one dominated by depressed mood and agitation. The mainstay of BD treatment has thus far been pharmacologic, but many patients remain severely disabled by their condition, despite the best available medical treatment. The successful use of deep brain stimulation (DBS) in movement disorders, and its promising results in major depressive disorder (MDD), has led researchers to consider its use in highly selected refractory cases of BD. Evidence form the imaging and circuitry literature suggests that similar underlying dyfunctional anatomic structures subserve both MDD and BD, indicating that modulation of key structures, can lead to an amelioration of symptoms and mood stabilization. Here, we propose a phase I clinical trial to evaluate the safety of DBS in BD.

NCT ID: NCT01473615 Active, not recruiting - Clinical trials for Major Depressive Disorder

Mindfulness Based Cognitive Therapy for Chronic Pain and Comorbid Unipolar Depression

Start date: November 2011
Phase: N/A
Study type: Interventional

The primary aim of this study is to test the feasibility and efficacy of Mindfulness Based Cognitive Therapy (MBCT) training for the treatment of depressive symptoms in patients with chronic pain. The study also aims to elucidate the mechanisms underlying MBCT on a psychological and neurobiological level. For this purpose the study subjects will fill out several psychological questionnaires related to mindfulness, depression and chronic pain. Moreover this study involves optional fMRI scans of the brain and blood measures before and after the intervention. Main hypotheses: 1. The MBCT training will be a feasible intervention in patients with chronic pain and co-morbid depression as defined by no occurrence of serious adverse events related to the intervention and a retention rate of more than 70% in the subjects assigned to the MBCT arm. 2. Patients who have completed the MBCT training will demonstrate a significant decrease in depressive symptoms as measured on the Quick Inventory of Depressive Symptomatology - Clinician rated (QIDS-C16), and the Hamilton Rating Scale for Depression (HRSD17) (QIDS-C/HRDS) severity scale for depressive symptoms (the primary outcome measure), compared to the control group.

NCT ID: NCT01473550 Completed - Mood Disorder Clinical Trials

Mental Health Engagement Network (MHEN)

MHEN
Start date: November 2011
Phase: N/A
Study type: Interventional

Patients with mood disorder or psychotic disorder will be given handheld devices with personal health records to educate, monitor and deliver customizable healthcare tools based on their personal needs. The use of technology has great potential to deliver care more effectively and efficiently. No actual information is on the handheld device - it is accessed from a secure site behind hospital firewalls.

NCT ID: NCT01473511 Completed - Clinical trials for Oppositional Defiant Disorder

Strongest Families Ontario (Formerly the Family Help Program)

SF-ON
Start date: February 2010
Phase: Phase 3
Study type: Interventional

Strongest Families (formerly Family Help)is an evidence-based, distance health education model for families who have children with behavioural difficulties. The principal research question is "Does Strongest Families, a 12-week, home-based program of interactive readings, instructional videos, homework projects, and weekly "coaching" telephone calls out perform the care families typically experience when referred to a mental health service?". The investigators hypothesize that children randomized to Strongest Families intervention will show a significantly greater reduction in externalizing behaviour problems than those randomized to a Control (usual care). In addition, parents randomized to Family Help will report a greater improvement in parenting skills and a greater reduction in symptoms of emotional distress (i.e., feeling of anxiety, depression, and stress) than parents in the Control condition. Finally, families randomized to Family Help will use fewer mental health services than Controls.

NCT ID: NCT01470781 Completed - Bipolar Disorder Clinical Trials

Treatment to Enhance Cognition in Bipolar Disorder

TREC-BD
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of the present study is to evaluate a neuroplasticity-oriented, computer-based cognitive remediation treatment program in patients with bipolar disorder and its effects on cognitive deficits and community functioning compared to an active, computer-based control.