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NCT ID: NCT00890240 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Study to Evaluate Pharmacokinetics, Safety and Tolerability After a Single Dose Administration of of JNJ-31001074 in Children (6-11 Years) With Attention Deficit Hyperactivity Disorder (ADHD)

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

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (process by which JNJ-31001074 is absorbed, distributed, metabolized, and eliminated by the body) after a single dose of JNJ-31001074. Up to three dose strengths will be tested in patients 6-11 years old with attention deficit hyperactivity disorder (ADHD).

NCT ID: NCT00889005 Completed - Clinical trials for Stress Disorder - Post-traumatic (Acute)

Prevention of Post-traumatic Stress Disorder by Telephone Based Cognitive Behavioral Therapy

Start date: May 2009
Phase: N/A
Study type: Interventional

This is a randomized controlled study comparing telephone-based cognitive behavioral therapy (CBT) for recent survivors of traumatic events with Acute Stress Disorder (ASD) or acute PTSD with a waitlist control group. Survivors with PTSD from both groups will receive face-to-face CBT one month from the traumatic event. The study's main hypothesis is that early telephone-based CBT will reduce the prevalence of PTSD three and eight months after the traumatic event.

NCT ID: NCT00888264 Completed - Bipolar Disorders Clinical Trials

A NIS Evaluating the Treatment Patterns of Atypical Antipsychotics in Patients Diagnosed With Bipolar I or II Disorder

HARMONY
Start date: May 2009
Phase: N/A
Study type: Observational

The purpose of this NIS is to obtain data on how AAPs are used in DSM-IV-TR Bipolar I and II Disorder, in the course of a major depressive episode. Both the parameters of use of AAPs and clinical evaluation will be recorded and potential differences that may exist due to epidemiological factors or comorbidities will be analyzed.

NCT ID: NCT00886886 Completed - Clinical trials for Substance-related Disorders

Interaction Between Reboxetine and 3,4-Methylenedioxymethamphetamine: Pharmacodynamics (PD) and Pharmacokinetics (PK)

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

MDMA releases dopamine, serotonin, and norepinephrine in the brain. Serotonin uptake inhibitors have been shown to interact with 3,4-Methylenedioxymethamphetamine (MDMA) and to decrease its psychoactive and cardiovascular stimulant effects. This finding indicates that MDMA acts in part by releasing serotonin through the serotonin uptake site. However, in vitro studies show that MDMA binds more potently to the norepinephrine uptake site that to the the serotonin or dopamine uptake transporter. In addition, norepinephrine uptake site blockers such antidepressant drugs attenuate some of the behavioral effects of MDMA in animals. These preclinical data indicate that norepinephrine may also contribute to the response to MDMA in humans. To test this hypothesis this study evaluates the interacting effects of the selective norepinephrine transporter inhibitor reboxetine on the subjective and cardiovascular stimulant effects of MDMA in healthy volunteers.

NCT ID: NCT00883519 Completed - Clinical trials for Major Depressive Disorder

The Efficacy of Parent Involvement in the Treatment of Adolescent Depression

Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The primary aim of this study is to examine whether adolescent depression and the family context in which it develops is best treated using an individual adolescent intervention or an intervention that includes both the adolescent and the parents. This will be accomplished by conducting a randomized controlled pilot study of Interpersonal Psychotherapy for Depressed Adolescents (IPT-A) in comparison to Interpersonal Psychotherapy for Depressed Adolescents and Parents (IPT-AP).

NCT ID: NCT00880217 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Study to Evaluate 3 Different Doses of JNJ-31001074 in the Treatment of Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety/tolerability of 3 different dosages of JNJ-31001074 compared with placebo in adult patients with attention-deficit/hyperactivity disorder (ADHD).

NCT ID: NCT00879515 Completed - Anxiety Disorders Clinical Trials

Examining Social, Emotional, and Cognitive Functioning in People With Fragile X and Down Syndromes

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

By testing physiological responses to anxiety in people with nervous system developmental disorders, this study will identify specific physiological characteristics associated with response to anxiety treatments.

NCT ID: NCT00873509 Completed - Autistic Disorder Clinical Trials

Buspirone in the Treatment of 2-6 Year Old Children With Autistic Disorder

B-ACE
Start date: May 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effects of twice-daily oral buspirone on core features of autism in autistic children aged 2-6 years as measured by the change from baseline in the Autism Diagnostic Observation Schedule (ADOS) Composite Total scores compared to placebo at 6 months.

NCT ID: NCT00870727 Completed - Clinical trials for Pervasive Developmental Disorder

Study of Aripiprazole in the Treatment of Pervasive Developmental Disorders

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

The purpose of this study is to develop a better tolerated and more effective pharmacologic treatment with individuals with Pervasive Developmental Disorder. This is a double-blind, placebo-controlled study of aripiprazole in the management of the maladaptive behaviors of Pervasive Developmental Disorder. The investigators hypothesize that aripiprazole will be more effective than placebo for reducing aggression, tantrum and self-injurious behavior in children with Pervasive Developmental Disorder.

NCT ID: NCT00870545 Completed - Combat Disorders Clinical Trials

Reintegration: The Role of Spouse Telephone BATTLEMIND Pilot Study

Start date: September 2009
Phase: N/A
Study type: Interventional

This study will expand the Department of Defense (DoD) one time, face-to-face post deployment BATTLEMIND training for spouses of Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Guard/Reserve service members into year-long, telephone groups focusing on education, skills building and support. The goal is to build spouses' resilience to cope with reintegration, help them serve as a support system for returning service members, and ease the transition for families post-deployment.