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Schizophrenia clinical trials

View clinical trials related to Schizophrenia.

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NCT ID: NCT00409201 Recruiting - Schizophrenia Clinical Trials

Reboxetine Adjuvant Therapy for the Treatment of Schizophrenia

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

30 patients will randomly be selected and will be administered either reboxetine or a placebo. changes in cognition and behavior will be assessed by computer tests and scales during a six week study period.

NCT ID: NCT00352339 Recruiting - Schizophrenia Clinical Trials

The New Strategy for Pharmacological Treatment in People With Schizophrenia

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

Switching from Risperidone to Aripiprazole in early stage of pharmacotherapy will demonstrate the same efficacy as compared to risperidone continuation treatment in the treatment of schizophrenia.

NCT ID: NCT00330226 Recruiting - Schizophrenia Clinical Trials

Efficacy and Safety of Psychopharmacotherapy in Patients With Schizophrenia or Bipolar Disorders

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the efficacy and safety of long-term psychopharmacotherapy in schizophrenia or bipolar disorder in terms of psychopathology and side effects.

NCT ID: NCT00305474 Recruiting - Schizophrenia Clinical Trials

Identification and Treatment of the Liability to Develop Schizophrenia

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

This study seeks to determine whether adult, non-psychotic, first-degree relatives of schizophrenic patients who show specific neurocognitive deficits and negative symptoms will show improvements in these areas following a 6-month, double-blind trial of a low dose (up to 2.0 mg) of risperidone.

NCT ID: NCT00300651 Recruiting - Schizophrenia Clinical Trials

Trial of Cognitive Behavioral Therapy for Schizophrenia

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

The following study addresses the hypothesis that cognitive-behavioral interventions will be effective in reducing positive and negative symptoms of schizophrenia under the conditions of the German health care system. It is also hypothesized that interventions designed to reduce delusions will reduce cognitive biases and dysfunctional self-concepts.

NCT ID: NCT00237809 Recruiting - Schizophrenia Clinical Trials

D-Serine Treatment of Negative Symptoms and Cognitive Deficits in Schizophrenia

Start date: September 2002
Phase: Phase 3
Study type: Interventional

This study is based on the hypothesis that by increasing N-methyl-D-aspartic acid (NMDA) receptor function in the brain and thereby increasing the capacity of the brain to both form new connections and strengthen existing connections, schizophrenic patients may derive both greater and sustained benefit from cognitive retraining.

NCT ID: NCT00231101 Recruiting - Clinical trials for Smoking Behavior in Schizophrenia

Quetiapine Decreases Smoking in Patients With Chronic Schizophrenia

Start date: January 2004
Phase: N/A
Study type: Interventional

A single-blind switching study in which forty subjects currently being treated with risperidone will be randomly assigned to either stay on risperidone or switched to quetiapine. Various behavioral and biological measures will be used to compare smoking behavior over time in these two groups.

NCT ID: NCT00215917 Recruiting - Schizophrenia Clinical Trials

D-Serine Monotherapy for Schizophrenia

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

N-methyl-D-aspartate receptor (NMDAR) agonist, added to classical or atypical antipsychotic medication, has reduced negative, depressive, and cognitive symptomatology. We will be investigating the effect of D-serine, (DSR), a selective and potent NMDAR agonist, as monotherapy for treatment resistant schizophrenics. 40 subjects on stable doses of risperidone will be randomized under double-blind conditions into a treatment group, which will receive D-serine 2100 mg, or a control group, which will continue to receive risperidone. Treatment will continue for 14 weeks. Symptoms and side effects will be rated biweekly with the CGI, PANSS, BPRS, SAS, AIMS, and UKU. Before and after the trial subjects will undergo neuropsychological assessments. Baseline and post-trial levels of amino acids relevant to glutamatergic neurotransmission (glutamate, glutamine, aspartate, glycine, serine, alanine) will be assessed. The primary outcome measures of the study will be the PANSS total scores and the positive and negative symptom cluster scores.

NCT ID: NCT00186771 Recruiting - Schizophrenia Clinical Trials

Magnetic Stimulation as a Treatment for Auditory Hallucinations in Schizophrenia

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

Schizophrenia is a chronic, severe, and disabling brain disease. Auditory hallucinations are the most frequent symptoms with an incident of 50% to 70% in patients. Transcranial Magnetic Stimulation (TMS) can significantly reduce symptoms of schizophrenia. TMS is capable of inducing changes in the electrical activities of the brain in humans. The purpose of this trial is to study the use of TMS to decrease auditory hallucinations in schizophrenia.

NCT ID: NCT00182494 Recruiting - Schizophrenia Clinical Trials

Diabetes Prevention Program in Schizophrenia [DPPS]

Start date: February 2005
Phase: Phase 4
Study type: Interventional

Diabetes is 2-5 times more common in schizophrenia and it is a preventable; but the current diabetes prevention guidelines are not suitable for implementation in the severely mentally ill population. The principles of diabetes prevention are essentially dietary regulation, increased physical activity and adjunctive use of oral anti-diabetic drugs (metformin). In a modified diabetes prevention protocol suitable for use in mentally ill population, we packaged the original guide lines with an adventure and recreation program based on principles of experiential learning, cognitive restructuring and behaviour modification. In this proposed study, we plan to evaluate the feasibility of adopting the new protocol, and examine its effectiveness in preventing diabetes.