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NCT ID: NCT02470026 Completed - Clinical trials for Major Depressive Disorder

Noradrenergic Activity, Cognition and Major Depressive Disorder

YohCog
Start date: June 2014
Phase: N/A
Study type: Interventional

This study investigates influences of nordadrenergic activity on cognition in patients with major depression regarding influences of early life stress.

NCT ID: NCT02469363 Completed - Clinical trials for Heart Rate and Rhythm Disorders

Hemodynamic Responses of Different Laryngoscopes

Start date: August 2014
Phase: Phase 4
Study type: Interventional

During laryngoscopy and endotracheal intubation, stimulation of supraglottic regions leads to an increase in the plasma catecholamine concentrations due to the activation of the sympatho-adrenal system. Prevention or reduction of this increment is important for hemodynamic control. Therefore, various methods such as providing adequate depth of anesthesia and shortening the time of laryngoscopy were used. On the other hand; alternative laryngoscopy devices and techniques have recently started to be used. In this randomized single blind study, the aim is to compare the hemodynamic responses of four different laryngoscopy techniques with Macintosh laryngoscope, McCoy laryngoscope, C-Mac videolaryngoscope and McGrath videolaryngoscope in patients with normal predictive airway.

NCT ID: NCT02466477 Completed - Depression Clinical Trials

Pharmacogenomic Decision Support With GeneSight Psychotropic to Guide the Treatment of Major Depressive Disorder

Start date: June 2015
Phase: Phase 4
Study type: Interventional

Evidence exists supporting the ability of genetic variations to influence patient drug response and side effects. Previous studies utilizing an open-label design have shown significant improvement in major depressive disorder (MDD) patient outcomes following use of the GeneSight Psychotropic (GEN) test. The first objective of this trial is to utilize a double-blinded, randomized clinical trial design to replicate previous findings of improvement in clinical outcomes in MDD subjects whose medication therapy was guided by GEN testing. Another objective is to determine the added benefit of Enhanced-GeneSight (E-GEN) compared to GEN for the pharmacogenomic guidance of treatment selections. Furthermore, this trial intends to develop an evidence-based case for the value of GEN and E-GEN to Canadian healthcare payers.

NCT ID: NCT02465697 Completed - Clinical trials for Borderline Personality Disorders

Changes in the Brain as Borderline Patients Learn to Regulate Their Emotions

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

Borderline Personality Disorder (BPD), a prevalent psychiatric disorder found in approximately 2% to 6% of the population and 20% of hospitalized psychiatric patients, has proven quite treatment resistant. This study is designed to determine whether patients with BPD can be trained to improve their ability to regulate their emotions and whether this leads to changes in how their brans regulate emotion.

NCT ID: NCT02464345 Completed - Bulimia Nervosa Clinical Trials

Healthy Approach to weIght Management and Food in Eating Disorders (HAPIFED)

HAPIFED
Start date: July 7, 2015
Phase: N/A
Study type: Interventional

The investigators have developed a new integrated therapy, namely a Healthy Approach to weIght management and Food in Eating Disorders (HAPIFED). HAPIFED is an enhanced behavioral weight loss therapy integrated with CBT for the management of EDs. HAPIFED uses CBT to treat ED behaviors and body image distress, whilst simultaneously emphasize a healthy lifestyle, the role of food and physical activity in mood regulation, and revised but clinically meaningful goals for weight loss. The investigators propose a randomized controlled trial (RCT) that will compare HAPIFED to CBT-E in people with obesity and either BN or BED. The two main aims will be to reduce symptoms of ED and to improve weight management. The RCT will be conducted in Sydney and in São Paulo with a one year follow-up.

NCT ID: NCT02460536 Completed - Anxiety Disorders Clinical Trials

Attention Bias Modification Treatment (ABMT) for Anxiety Disorders in Youth

Start date: May 2015
Phase: N/A
Study type: Interventional

Attention biases in threat processing have been assigned a prominent role in the etiology and maintenance of anxiety disorders. Attention Bias Modification Treatment (ABMT) utilizes computer-based protocols to implicitly modify biased attentional patterns in anxious patients. This is a double-blind randomized controlled trial of ABMT for clinically anxious 10-18 year-olds. Participants will be assessed using clinical interviews and parent- and self-rated questionnaires before, in the middle and after twelve sessions of ABMT or control groups, and again at ten-week follow-up. Outcome measures will be anxiety symptoms and depression as measured by gold standard questionnaires as well as structured clinical interviews with youth and their parents. Attentional threat bias, Attentional control and interpretation of ambiguous information will also be measured to explore potential mediators of ABMT's effect on anxiety. The investigators expect the findings to inform pathways to treatments for anxious children and to provide initial information on mechanisms of ABMT efficacy.

NCT ID: NCT02459340 Completed - Clinical trials for Dissociative Disorder Not Otherwise Specified (DDNOS)

Emotional and Cognitive Self-regulation, an EEG Study

ECSR
Start date: June 2015
Phase: N/A
Study type: Interventional

The main goal of the proposed project is to assess treatment-induced changes of electrophysiological and psychophysiological correlates of the capacity to regulate emotion, executive functions, and clinical measures in individuals with complex posttraumatic stress disorder and dissociative disorders in a naturalistic inpatient setting.

NCT ID: NCT02457052 Completed - Clinical trials for Deglutition Disorders

Impact of a Transportable Customizable and Scalable Sitting Positioning Device on Swallowing Disorders

DATP-DEG
Start date: October 2014
Phase: N/A
Study type: Interventional

When the seat is a vehicle for disabled person, postural adaptation methodology is known and, on prescription, there is possibility of financial support for technical posture assists. For people who use a standard seat, a chair for example, there is no satisfactory existing hardware. A transportable customisable and scalable sitting positioning device (DATP device), to be placed on a standard seat, is a solution that might fit in the home, in specialized foster homes or in institutions for the elderly. Such a device has been developed but earnings on swallowing disorders have to be validated.

NCT ID: NCT02456896 Completed - Bipolar Disorder Clinical Trials

Effect of Oxcarbazepine on Serum Brain Derived Neurotrophic Factor (BDNF) in Bipolar Disorder

Start date: June 2015
Phase: Phase 4
Study type: Interventional

The present study has been designed to evaluate the change in serum BDNF level with oxcarbazepine monotherapy in bipolar disorder and to explore the possibility of its neuroprotective effect.

NCT ID: NCT02456454 Completed - Bipolar Disorder Clinical Trials

Controlled Trial of Valproate Versus Risperidone in Young Children With Bipolar Disorder

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

Controlled trial of the efficacy and safety of valproate, versus risperidone in children, ages 3-7 yr. with Bipolar I or II Disorder, mixed, manic or hypomanic episode.