Clinical Trials Logo

Disease clinical trials

View clinical trials related to Disease.

Filter by:

NCT ID: NCT00457899 Terminated - Schizophrenia Clinical Trials

Rapid Versus Conventional Titration of Quetiapine in Schizophrenia/Schizoaffective Disorder

RAPID
Start date: July 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether increasing the amount (dose) of quetiapine IR (immediate release formulation) more rapidly than conventional dose increases, improves the control of symptoms as measured by the Positive and Negative Syndrome Scale (PANSS) - a psychiatric assessment scale that measures both positive and negative symptoms - in patients with acute schizophrenia or schizoaffective disorder.

NCT ID: NCT00451542 Terminated - Bipolar Disorder Clinical Trials

Divalproex vs. Lamotrigine for Bipolar Disorder

Start date: February 1, 2006
Phase: N/A
Study type: Observational

This study is a retrospective chart review of patients treated for bipolar disorder at the TVAMC in the past four years cross-referenced with the electronic pharmacy file for having received a prescription of divalproex or lamotrigine.

NCT ID: NCT00400933 Terminated - Eating Disorders Clinical Trials

Evaluation of a Six-session Psycho-education Group Program

Start date: November 2006
Phase: Phase 1
Study type: Interventional

The aim of this project is to analyze the impact of a psycho-educational group program on the family members and close friends of persons with eating disorders and co-morbid personality disorders.

NCT ID: NCT00400088 Terminated - Clinical trials for Major Depressive Disorder

Lithium Versus Paroxetine in Patients With Major Depression Who Have a Family History of Bipolar Disorder or Suicide

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

This study is being done to look at how well people respond to two very different drug treatments for depression. Clinically, people with depression can respond differently to drug treatments for reasons which are not always clear. Some of our own recent research suggests that people with depression who have a family history of bipolar disorder or completed suicide, may react differently to standard antidepressant medications than those without such a family history. Our data shows that family history of completed suicide, as well as the known predictor of family history of bipolar disorder, may help identify a pre-bipolar high risk group i.e. they currently have depression but at some future date will declare a bipolar illness (manic-depression) by virtue of development of a manic episode also. Our research suggests that treatment- emergent symptoms in response to a trial of antidepressant, such as agitation may be strong predictors of future bipolarity and inherently dangerous particularly as they are not ascribed to the antidepressant treatment. Finally, it is possible that this subgroup of those with depressive illness may respond better and more safely to lithium, a mood stabiliser used in known bipolar depression. The objective of this proposal is to investigate response to acute lithium treatment in subjects who meet the diagnostic criteria for major depression, but who are potentially at risk for bipolar disorder, by virtue of family history of bipolarity or completed suicide.

NCT ID: NCT00374543 Terminated - Bipolar Disorder Clinical Trials

Ziprasidone for the Treatment of Generalized Anxiety in Patients With Bipolar Disorder

Start date: February 2006
Phase: Phase 4
Study type: Interventional

This study proposes to examine the potential safety and efficacy of ziprasidone for patients with anxiety and bipolar disorder on anxiety outcomes, bipolar symptoms, and on measures of quality of life and resilience.

NCT ID: NCT00359398 Terminated - Clinical trials for Cardiopulmonary Bypass

Sequestration of Platelets Prior to Bypass Reduces Bleeding After Cardiac Surgery

Start date: August 2006
Phase: Phase 2
Study type: Interventional

Excessive bleeding is common after cardiac surgery. This may result in patients receiving a blood transfusion or suffering the life-threatening complication of cardiac tamponade. Tamponade is when excessive bleeding compresses the heart and prevents it from pumping properly. A major reason for the bleeding is the damage done to platelets by the cardiopulmonary bypass (CPB) machine. Often patients receive platelets and plasma from blood donors to try to reduce the bleeding post-operatively. The investigators plan to take platelets and plasma from patients before they are damaged. They would then return these 'undamaged' sequestered platelets to the patients after the bypass machine is no longer needed. Therefore, the investigators' primary question is whether platelet sequestration would reduce the bleeding problems that occur following cardiac surgery. They will evaluate bleeding problems using thromboelastography, which provides a comprehensive assessment of both how blood clots form and their strength. If sequestration reduces bleeding problems following cardiac surgery then it may reduce the chance of patients receiving blood products from donors. Although donated blood is thoroughly tested, its use does expose patients to the risk of transfusion errors, blood borne infections and reactions. Avoiding its use would be very desirable.

NCT ID: NCT00358657 Terminated - Clinical trials for Severe Aplastic Anemia

Fludarabine Phosphate, Cyclophosphamide, and Total-Body Irradiation Followed by Donor Bone Marrow Transplant and Cyclophosphamide, Mycophenolate Mofetil, Tacrolimus, and Sirolimus in Treating Patients With Primary Immunodeficiency Disorders or Noncancerous Inherited Disorders

Start date: May 24, 2006
Phase: Phase 2
Study type: Interventional

This phase I/II trial studies the side effects of fludarabine phosphate, cyclophosphamide and total-body irradiation followed by donor bone marrow transplant and cyclophosphamide, mycophenolate mofetil, tacrolimus, and sirolimus in treating patients with primary immunodeficiency disorders or noncancerous inherited disorders. Giving low doses of chemotherapy and total-body irradiation before a bone marrow transplant helps prepare the patient's body to accept the incoming donor's bone marrow and decrease the risk that the patient's immune system will reject the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells called graft versus host disease. Giving cyclophosphamide, mycophenolate mofetil, tacrolimus, and sirolimus after the transplant may help decrease this from happening.

NCT ID: NCT00353379 Terminated - Clinical trials for Personality Disorders

Pharmacology of Cognition in Schizotypal Personality Disorder

Start date: September 1995
Phase: Phase 4
Study type: Interventional

This study will determine the effectiveness of guanfacine in improving cognitive and functional impairments in schizotypal personality disorder.

NCT ID: NCT00314327 Terminated - Schizophrenia Clinical Trials

Optimizing Response in Psychosis Study

ORP
Start date: April 2006
Phase: Phase 4
Study type: Interventional

The purpose of this project is to evaluate the efficacy of long-acting risperidone for patients with first episode schizophrenia spectrum who did not improve sufficiently with the first antipsychotic medication they tried during their initial treatment trial.

NCT ID: NCT00288353 Terminated - Schizophrenia Clinical Trials

Estimating and Reducing the Cardiovascular Risk of Patients With Schizophrenia Drugs From Lipid Measures and Ischemic Electrocardiographic Changes

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

The primary goal of this study is to examine the triglyceride/HDL ratio and the ischemic EKG changes in patients with schizophrenia, schizoaffective disorder or bipolar disorder.