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NCT ID: NCT00538122 Completed - Schizophrenia Clinical Trials

Changes in Heart Rhythms Associated With Antipsychotic Drug Treatment

Start date: July 2007
Phase: N/A
Study type: Observational

This study is being done to look at the electrical activity of the heart. This study will help decide whether taking recordings for a 24-hour period gives more useful information than recording it for a few seconds in a doctor's office. The study will compare 24 hour electrocardiogram (ECG) results of patients taking thioridazine (Mellaril) to those of other patients taking different medications that took part in another study.

NCT ID: NCT00537940 Completed - Epilepsy Clinical Trials

Comparative Study Of Pregabalin And Gabapentin As Adjunctive Therapy In Subjects With Partial Seizures

Start date: February 2008
Phase: Phase 4
Study type: Interventional

To compare the efficacy of pregabalin and gabapentin, as adjunctive therapy in subjects with partial seizures.

NCT ID: NCT00537758 Completed - Obesity Clinical Trials

Treatment for Obesity and Binge Eating Disorder

Start date: July 2002
Phase: N/A
Study type: Interventional

This study is a test of cognitive behavioral therapy(CBT) and behavioral weight loss (BWL) treatments for obese patients with binge eating disorder (BED). The study involves a comparison of three treatment conditions: (1) CBT; (2) BWL, and (3) a sequential (two-part) treatment consisting of CBT followed by BWL.

NCT ID: NCT00535145 Completed - Schizophrenia Clinical Trials

Study to Measure the Safety of Paliperidone ER (Extended-release) in Patients With Liver Disease

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the tolerability and safety of paliperidone ER (extended-release) in doses between 3 milligrams per day and 12 milligrams per day in the treatment of patients with schizophrenia or schizoaffective disorder and liver disease.

NCT ID: NCT00534599 Completed - Anxiety Clinical Trials

Generalized Anxiety Disorder Adjunct Study

Start date: August 2007
Phase: Phase 3
Study type: Interventional

This study is being carried out to see if extended release quetiapine fumarate (Seroquel®XL) when added to standard selective serotonin reuptake inhibitor (SSRI) / serotonin-norepinephrine reuptake inhibitor (SNRI) therapy is effective and safe for the treatment of Generalized Anxiety Disorder in patients with partial or no response to SSRI/SNRI alone or in combination with a benzodiazepine, and if so, how it compares with placebo

NCT ID: NCT00533923 Completed - Multiple Myeloma Clinical Trials

Nonmyeloablative Allogeneic Stem Cell Transplantation From HLA-Matched Unrelated Donor for the Treatment of Hematologic Disorders

Start date: December 2002
Phase: Phase 2
Study type: Interventional

Allogeneic stem cell transplantation may provide long-term remissions for some patients with hematological malignancies. However, allogeneic transplantation is associated with a significant risk of potentially life threatening complications due to the effects of chemotherapy and radiation on the body and the risks of serious infection. In addition, patients may develop a condition called Graft versus host disease that arises from an inflammatory reaction of the donor cells against the recipient's normal tissues. The risk of graft versus host disease is somewhat increased in patients who are receiving a transplant from an unrelated donor. One approach to reduce the toxicity of allogeneic transplantation is a strategy call nonmyeloablative or "mini" transplants. In this approach, patients receive a lower dose of chemotherapy in an effort to limit treatment related side effects. Patients undergoing this kind of transplant remain at risk for graft versus host disease particularly if they receive a transplant from an unrelated donor. The purpose of this research study is to examine the ability of a drug called CAMPATH-1H to reduce the risk of graft versus host disease and make transplantation safer. CAMPATH-1H binds to and eliminates cells in the system such as T cells that can cause graft versus host disease (GvHD). As a result, earlier studies have shown that patients who receive CAMPATH-1H with an allogeneic transplant have a lower risk of GvHD. In the present study, we will examine the impact of treatment with CAMPATH-1H as part of an allogeneic transplant on the development of GvHD and infection. In addition, we will study the effects of CAMPATH-1H on the immune system by testing blood samples in the laboratory.

NCT ID: NCT00531518 Completed - Depression Clinical Trials

Early Detection and Intervention for the Prevention of Psychosis

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

EDIPP is a multisite trial of early identification and intervention to prevent the onset of psychosis in adolescents and young adults, carried out at six sites across the United States. The hypothesis is that very early identification and intervention will be effective in delaying or preventing onset of psychosis and improving social and occupational functioning.

NCT ID: NCT00529906 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Endophenotype, Molecular Genetic Study on Attention-Deficit/Hyperactivity Disorder

Start date: August 2007
Phase:
Study type: Observational

The ultimate goals of this study are to identify patterns of familial aggregation with regards to categorical and dimensional approaches of ADHD and neuropsychological measures, to validate the phenotypes and endophenotypes that are close to biological expression of genders underlying ADHD, and to identify the genetic variants close to the etiological genes of ADHD in Taiwanese sample. We propose to replicate the analysis of the candidate genes identified by previous genetic studies on ADHD using the candidate gene association study design (family-based case control study using parental controls) to validate the findings from other research groups. With the accomplishment of these goals, this study will resolve controversies over inconsistent findings in previous genetic studies and contribute to the literature on the validity of ASD using clinical and genetic data.

NCT ID: NCT00529217 Completed - Clinical trials for Depersonalization Disorder

Treatment of Depersonalization Disorder With Transcranial Magnetic Stimulation (TMS)

TMS
Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the clinical efficacy of transcranial magnetic stimulation in the treatment of Depersonalization Disorder (DPD).

NCT ID: NCT00525226 Completed - Depression Clinical Trials

Evaluating the Effects of Stress in Pregnancy

Start date: September 2007
Phase: N/A
Study type: Observational

This study will evaluate pregnant women with a past or current diagnosis of depression or anxiety to gain a better understanding of how these disorders can affect an infant's development, both during and after pregnancy.