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Schizophrenia, Paranoid clinical trials

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NCT ID: NCT01190254 Completed - Clinical trials for Schizophrenia, Paranoid

Fixed Dose Efficacy and Safety Study of Asenapine for the Treatment of Schizophrenia in Adolescents (P05896)

Start date: September 28, 2010
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate whether asenapine, which is approved by the United States Food and Drug Administration (US FDA) for acute treatment of schizophrenia in adults, is also effective in adolescents with schizophrenia. Participants who qualify for the study will be randomly assigned to receive a fixed dose of asenapine (either 2.5 mg or 5 mg twice daily [BID]) or placebo for 8 weeks. Throughout the study, observations will be made on each participant at various times to assess the efficacy and safety of the study treatment. The primary objective of the trial is to demonstrate significant superiority of at least one asenapine dose to placebo, as measured by the change from baseline of the Positive and Negative Syndrome Scale (PANSS) total score at Day 56.

NCT ID: NCT00716755 Completed - Schizophrenia Clinical Trials

Minimizing Doses of Antipsychotic Medication in Older Patients With Schizophrenia.

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

Since side effects of antipsychotics, dopamine D2 receptor blockers, frequently occur in older patients with schizophrenia and the risk is dose dependent, clinical guidelines universally advocate the use of lower doses. However, there is no report to test this dosing guideline with measurements of D2 receptor blockade caused by antipsychotics. In this study, dopamine D2 receptor occupancy will be measured, using Positron Emission Tomography (PET), in 40 patients aged 50 and older with schizophrenia-spectrum disorders before and after a gradual 40 % dose reduction of antipsychotics that was safely achieved in the past study while setting a target dose still above the lower limit of the dose range recommended in clinical guidelines for older patients. Our goal is to relate changes in clinical outcome, including subjective and objective clinical ratings, to dopamine D2 receptor occupancy, and compare these results with the data for younger patients in the literature.

NCT ID: NCT00644800 Completed - Schizophrenia Clinical Trials

A Study of the Efficacy and Safety of Intramuscular Ziprasidone Followed by Oral Ziprasidone for the Treatment of Psychosis

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

To assess the efficacy, safety, and tolerability of intramuscular ziprasidone in the treatment of the acute exacerbation of non-organic psychosis of any etiology, including schizophrenia, acute mania, delusional disorder and others.

NCT ID: NCT00506077 Completed - Clinical trials for Paranoid Schizophrenia

MK0249 for the Treatment of Cognitive Impairment in Patients With Schizophrenia (0249-016)

Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of an investigational drug MK0249 for the treatment of the cognitive impairment in patients with schizophrenia.

NCT ID: NCT00482430 Completed - Schizophrenia Clinical Trials

MK0557 for the Treatment of Cognitive Impairment in Patients With Schizophrenia (0557-027)

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of an investigational drug for the treatment of cognitive impairment in patients with schizophrenia.

NCT ID: NCT00222807 Completed - Schizophrenia Clinical Trials

Schizophrenia, Antipsychotic Treatment and the Risk for Diabetes Mellitus

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

This preliminary study aims to investigate the mechanism of higher rates of type 2 diabetes mellitus in patients with schizophrenia. As part of the study, we collect neuroendocrine-immune data on patients with first episode, treatment naive psychosis, patients with newly diagnosed schizophrenia and normal healthy controls. Regardless the treatment status, we collect the same neuroendocrine-immune data on the participants after 2 months.