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NCT ID: NCT00953862 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Atomoxetine/Attention Deficit/ Hyperactive Disorder (ADHD)/Substance Use Disorder (SUD)in a Residential Treatment Facility

Start date: July 2005
Phase: N/A
Study type: Interventional

Although Attention Deficit/ Hyperactive Disorder (ADHD) is a common comorbidity in individuals diagnosed with Substance Use Disorder (SUD), little data currently exists on the utility of screening tools in large samples of adult patients with SUD in inpatient treatment. This was a 10-week, 2-phase, open label trial of atomoxetine for ADHD in adult patients being treated for a co-morbid SUD in a residential treatment facility (RFT). The primary objective of the study was to assess the efficacy of atomoxetine in adults with an SUD and ADHD. Secondary objects included assessment of the co-morbidity of ADHD and the safety and tolerability of atomoxetine in this population.

NCT ID: NCT00953693 Completed - Hepatic Disorders Clinical Trials

Patient Specific Induced Pluripotency Stem Cells (PSiPS)

Start date: April 2009
Phase: N/A
Study type: Observational

Induced pluripotent stem cells (iPSCs) are adult cells that have been genetically reprogrammed to an embryonic stem cell-like state by being forced to express genes and factors important for maintaining the defining properties of embryonic stem cells. The reprogramming of adult cells into embryonic stem (ES) cells enables the generation of patient-specific stem cells and thus has enormous potential for the treatment and analysis of degenerative diseases. In this project the investigators are going to induce pluripotent stem cells from cell cultures from skin biopsies of patients. The iPS cells will be developed for modeling diseases and drug discovery as well as basic research.

NCT ID: NCT00953654 Completed - Clinical trials for Generalized Anxiety Disorder

Exercise Training for the Treatment of Generalized Anxiety Disorder

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

The purpose of this study is to compare the effects of 6 weeks of endurance or strength training and a wait list comparison condition on symptoms of Generalized Anxiety Disorder (GAD).

NCT ID: NCT00952185 Terminated - Lymphoma Clinical Trials

Influenza Vaccine in Preventing Flu in Patients Who Have Undergone Stem Cell Transplant and in Healthy Volunteers

Start date: November 2008
Phase: N/A
Study type: Interventional

RATIONALE: The influenza vaccine may help prevent flu in patients who have undergone stem cell transplant. PURPOSE: This clinical trial is studying how well the influenza vaccine works in preventing flu in patients who have undergone stem cell transplant and in healthy volunteers.

NCT ID: NCT00950885 Completed - Shift-work Disorder Clinical Trials

Melatonin Treatment for Induced Transient Insomnia

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

Melatonin supplements have been reported to be an effective treatment for circadian rhythm sleep disorders, including shift work dyssomnia, jet-lag, delayed sleep phase syndrome, and sleep disruption suffered by many blind individuals. However, the mechanism(s) by which melatonin affects the timing of sleep are not well-understood. The purpose of this study is to determine if melatonin improves sleep and performance on a schedule simulating eastward travel. This study will provide information regarding the mechanism of action of melatonin that will be critical for the use of melatonin as a treatment for circadian rhythm sleep disorders.

NCT ID: NCT00948974 Completed - Clinical trials for Social Anxiety Disorder

Variations of Cognitive Behavior Therapy for Social Anxiety Disorder

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of two variants of cognitive behavioral therapy (CBT) (cognitive therapy (CT) and acceptance and commitment therapy (ACT)), for the treatment of generalized social anxiety disorder.

NCT ID: NCT00947570 Completed - Anxiety Disorders Clinical Trials

Neural Functioning Underlying Anxiety and Its Treatment (The INSULA Study)

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

This study will examine the effects of cognitive behavioral therapy on brain function in people with anxiety disorders.

NCT ID: NCT00947544 Completed - Clinical trials for Urea Cycle Disorders

Study of the Safety and Tolerability of HPN-100 Compared to Sodium Phenylbutyrate in Children With Urea Cycle Disorders

Start date: March 2010
Phase: Phase 2
Study type: Interventional

Protocol HPN-100-005 was the first study of HPN-100 in pediatric subjects with urea cycle disorders (UCDs) and was a fixed-sequence, open-label, switch over study of HPN-100 with a long-term (12 month) safety extension designed to assess the safety of HPN-100 and to prospectively assess its ability to control blood ammonia as compared with Sodium Phenylbutyrate (NaPBA). Upon DSMB review of the first ten subjects who completed the switch over part of the study, and with DSMB approval, up to an additional 20 subjects were enrolled into the safety extension part of the study. HPN-100 is a triglyceride that has a similar mechanism of action as NaPBA. It is a liquid with minimal taste and odor. Three teaspoons of HPN-100 (~17.4mL) delivers an equivalent amount of PBA to 40 tablets of NaPBA.

NCT ID: NCT00947297 Completed - Clinical trials for Urea Cycle Disorders

Study of the Safety of HPN (Hyperion)-100 for the Long-Term Treatment of Urea Cycle Disorders (Treat UCD)

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

This was a long-term safety study HPN-100 in urea cycle disorder (UCD) subjects. Subjects were assessed regularly for safety and control of their venous ammonia. Hyperammonemic events were characterized with respect to contributing factors, such as intercurrent illness, diet, and noncompliance with medication.

NCT ID: NCT00946348 Completed - Schizophrenia Clinical Trials

Cannabis and Schizophrenia: Self-Medication and Agonist Treatment

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

The first aim of this study is to determine whether a brain reward center (BRC) deficiency in patients with schizophrenia (SCZ) and cannabis use disorder (CUD) will be normalized when patients are given cannabis or dronabinol. The second aim will serve to further assess the effects of dronabinol on symptoms and medication side effects in this population.