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Psychotic Disorders clinical trials

View clinical trials related to Psychotic Disorders.

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NCT ID: NCT00160147 Terminated - Clinical trials for Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

Start date: December 2005
Phase: Phase 3
Study type: Interventional

This is a 10-week study with bifeprunox and placebo in elderly subjects with psychosis and behavioral disturbances associated with dementia of the alzheimer's type.

NCT ID: NCT00159770 Completed - Schizophrenia Clinical Trials

Effect And Safety Of Ziprasidone Compared To Other Atypical Antipsychotic Drug In Schizophrenic Patients

Start date: November 2001
Phase: Phase 3
Study type: Interventional

Evaluation of the antipsychotic efficacy and safety of ziprasidone versus olanzapine, risperidone or quetiapine in patients with schizophrenia, schizoaffective and schizophreniform disorders under naturalistic conditions of clinical practice

NCT ID: NCT00159601 Completed - Mental Disorders Clinical Trials

Quality of Life and Mental Health in Children and Adolescents

Start date: June 2003
Phase: N/A
Study type: Observational

The purpose of this study is to investigate different aspects of Quality of Life and mental health in patients under treatment in a child and adolescent psychiatric outpatient clinic and in the normal population.

NCT ID: NCT00158223 Completed - Schizophrenia Clinical Trials

Effectiveness of Pimozide in Augmenting the Effects of Clozapine in the Treatment of Schizophrenia

Start date: October 2004
Phase: Phase 4
Study type: Interventional

This study will assess the effectiveness of pimozide in enhancing the effects of clozapine in the treatment of schizophrenia.

NCT ID: NCT00157313 Active, not recruiting - Clinical trials for Schizoaffective Disorder

Clinical Trial of Integrated Treatment Versus Standard Treatment in First Episode Psychosis

Start date: January 1998
Phase: N/A
Study type: Interventional

The purpose of the study was to evaluate the effects of integrated treatment for patients with a first episode of psychotic illness. We conducted a randomised clinical trial in Copenhagen Hospital Corporation and Psychiatric Hospital Aarhus, Denmark. We included 547 patients with first episode of schizophrenia spectrum disorder, who has not received antipsychotic medication for more than 12 weeks. Patients were randomised to integrated treatment or standard treatment. The integrated treatment lasted for two years and consisted of assertive community treatment with programmes for family involvement and social skills training. Standard treatment offered contact with a community mental health centre. We wanted to study the effect on psychotic (hallucinations and delusions)and negative (lack of initiative, apati, blunted affect) symptoms (each scored from 0 to a maximum of 5) at one and two years' follow-up. We found that integrated treatment improved clinical outcome and adherence to treatment. The improvement in clinical outcome was consistent at one year and two year follow-ups. We will study further outcome measures such as social network, quality of life, depression and suicidal behaviour.

NCT ID: NCT00156715 Completed - Schizophrenia Clinical Trials

Efficacy of Quetiapine in the Treatment of Patients With Schizophrenia and a Comorbid Substance Use Disorder

Start date: March 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the efficacy of quetiapine (Seroquel) in reducing substance use in persons diagnosed with schizophrenia. The primary hypothesis is that quetiapine treatment will be associated with a decrease in substance use.

NCT ID: NCT00156637 Completed - Schizophrenia Clinical Trials

A Study of Strategies to Improve Schizophrenia Treatment

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

The goal of this project is to translate research findings about key aspects of antipsychotic treatment into routine care through a multi-component intervention, focusing on improving two aspects of medication management that are directly linked to patient outcomes: 1) monitoring for potentially serious metabolic side effects of newer antipsychotic medication, and 2) increasing the appropriate use of clozapine for treatment-refractory patients.

NCT ID: NCT00148083 Completed - Schizophrenia Clinical Trials

Effects of Risperdal Consta on Ability to Benefit From Social Skills Training in Schizophrenia

Start date: September 2005
Phase: Phase 3
Study type: Interventional

The specific aim of this study is to determine whether the new, long-acting, form of risperidone, Risperdal Consta, improves the ability of schizophrenia patients to benefit from skills training. The hypothesis guiding this study is that Risperdal Consta, by improving verbal memory, will improve the ability to benefit from skills training interventions among schizophrenia patients. The primary objective of this study is to compare patients on Risperdal Consta to patients on other atypical antipsychotic medications in terms of their ability to benefit from skills training interventions. A secondary objective of this study is to determine whether patients taking Risperdal Consta improve in other areas of cognitive functioning and social functioning.

NCT ID: NCT00146523 Completed - Clinical trials for Major Depressive Disorder

An International Study of the Safety and Tolerability of Corlux for Psychotic Symptoms in Psychotic Major Depression

Start date: May 2005
Phase: Phase 3
Study type: Interventional

Corlux (mifepristone) is a new medication that modulates the body's use of a hormone called cortisol. Under normal conditions, cortisol and other hormones are created by the body in response to physical and emotional stress, triggering a healthy stress response. People who suffer from psychotic major depression may have unusually high levels of cortisol circulating within them or abnormal patterns of cortisol levels, overloading the stress response mechanism and causing symptoms of psychosis such as delusional thoughts or hallucinations. If Corlux can keep the body's cortisol receptors from being overloaded, the stress response system may return to normal function, which may result in improvement of symptoms. The purpose of this 56 day study is to learn the safety and effectiveness of Corlux in patients who have been diagnosed with psychotic major depression (PMD).

NCT ID: NCT00145847 Completed - Schizophrenia Clinical Trials

Naltrexone Treatment of Alcohol Abuse in Schizophrenia

Start date: April 2003
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to determine whether naltrexone is effective in the treatment of alcohol dependence and abuse in patients with schizophrenia and schizoaffective disorder. Hypotheses are as follows: hypothesis 1: Naltrexone will be more effective than placebo in reducing alcohol use. hypothesis 2: Patients responding to naltrexone by reducing alcohol use will also show reductions in severity of psychiatric symptoms and utilization of inpatient and emergency psychiatric services. hypothesis 3: Severity of psychiatric symptoms and amount of service utilization will correlate positively with alcohol use.