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Psychosis clinical trials

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NCT ID: NCT00591318 Terminated - Schizophrenia Clinical Trials

A Placebo-controlled Efficacy Study of IV Ceftriaxone for Refractory Psychosis

Start date: October 10, 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Many patients with schizophrenia and schizoaffective disorder have symptoms that persist, including hallucinations or delusions, despite adequate pharmacotherapy with antipsychotic drug. Glutamate is a major excitatory neurotransmitter in the brain that has been implicated in several brain diseases. NMDA antagonist drugs cause symptoms of psychosis in otherwise normal persons. It is postulated that reduced NMDA receptor mediated neurotransmission leads to an increase in synaptic glutamate. Excessive synaptic concentrations of glutamate can produce excitatory neurotoxicity. Agents which reduce excess glutamate activity are neuroprotective. This therapeutic strategy has been applied to schizophrenia through the use of compounds that reduce presynaptic release of glutamate or otherwise decrease excessive postsynaptic stimulation, including lamotrigine, memantine and a m-GLU-R2 agonist (LY354740) with the hypothesized result of a reduction in psychotic symptoms. Recently it was shown that a commonly available antibiotic (ceftriaxone) has the unique neuroprotective function of decreasing the amount of extracellular glutamate in nervous system tissue by increasing the number of glutamate transporter proteins. Our clinical experience with patients who have refractory psychosis and past Lyme disease indicates that in some patients psychosis may improve with IV ceftriaxone therapy. Whether this improvement was due to its antimicrobial or glutamate effect or a placebo effect is uncertain. In a placebo-controlled design, this study investigates the ability of ceftriaxone to decrease psychotic symptoms in patients with refractory psychotic disorders. In addition, the study will examine glutamatergic functional activity before and after treatment using brain imaging with magnetic resonance spectroscopy.

NCT ID: NCT00461318 Completed - Psychosis Clinical Trials

The Effectiveness of Supported Employment for People With Severe Mental Illness: an RCT in Six European Countries

EQOLISE
Start date: April 2003
Phase: N/A
Study type: Interventional

The primary aim of the study was to determine the effectiveness of a form of supported employment, Individual Placement and Support (IPS) compared to existing good quality rehabilitation and vocational services for people with psychotic illnesses in terms of ‘open’ employment outcomes (in the competitive labour market), and to examine its relative effectiveness in the context of different European welfare systems and labour markets. The primary hypothesis was that IPS patients would be more likely to obtain open employment than control service patients. Secondary hypotheses were that they would be in open employment for longer than the control patients, and that they would not spend more time in hospital.

NCT ID: NCT00449397 Completed - Psychosis Clinical Trials

Dose Finding of Quetiapine Fumarate 200mg vs 400mg in First Episode Psychosis

Start date: July 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is determine the minimal effective dose and the impact on: 1. treatment outcomes at 4, 12 and/or 48 weeks the treatment has required to treat patients experiencing the first psychotic episode 2. the final maintenance doses 3. the use of other medications 4. the amount of changes to other antipsychotic medication 5. the number of hospitalization days

NCT ID: NCT00421954 Completed - Bipolar Disorder Clinical Trials

Open-label Ziprasidone Study for Psychosis Treatment in Adolescents

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

This open-label study will assess the medication Geodon® (Ziprasidone) in pediatric patients, aged 13-17, diagnosed with psychotic disorder. Eligible adolescents will receive Geodon® for 7 weeks and stay at the NYSPI Children's Day Unit (CDU) during the day. If clinically appropriate, they may also stay at the New York State Psychiatric Institute (NYSPI) Schizophrenia Research Unit (SRU) inpatient facility.

NCT ID: NCT00407277 Completed - Schizophrenia Clinical Trials

Neural Inhibition as a Mechanism of Nicotine Dependence Among Persons With Schizophrenia

Start date: February 2007
Phase: N/A
Study type: Interventional

Cigarette smoking decreases life expectancy, causes devastating health complications, and costs society billions of dollars each year. These untoward consequences are especially pronounced among persons with schizophrenia (SCZ) because approximately 80% to 95% of this group smokes cigarettes. These high prevalence rates underscore the need for research investigating the determinants of smoking in patients with SCZ. Several researchers have observed that nicotine improves specific symptoms of SCZ including negative symptoms, negative affect, and cognitive deficits. This has led to the hypothesis that patients with SCZ smoke in an attempt to self-medicate. However, the mechanism(s) by which nicotine has its positive effect on symptoms remains unclear. The current proposal posits that neural inhibition (NI) is a physiological mechanism of this effect, while variation in the alpha-7-nicotinic receptor subunit gene (CHRNA7) represents the genetic underpinnings of these processes. The proposed study will assess NI and symptom improvement after acute administration of nicotine to both smokers and nonsmokers with SCZ. In addition, NI and CHRNA7 variation will be tested as predictors of patients' ability to reduce/quit smoking following smoking treatment. These data may lead to the development of new pharmacological strategies for treating the symptoms of SCZ and new methods for assisting these patients to quit smoking.

NCT ID: NCT00281320 Completed - Psychosis Clinical Trials

Study of Asenapine in Elderly Subjects With Psychosis (A7501021)(P05717)

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

This study evaluates the safety and tolerability of Asenapine in elderly patients with psychosis.

NCT ID: NCT00272597 Completed - Schizophrenia Clinical Trials

Risperidone LA Heathcare Resource Study

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

The primary objective of this pilot study is to evaluate the impact of switching 30 subjects from an existing antipsychotic to risperidone long acting on healthcare resource utilization. The study will be a ten month open-label, 'mirror-image', pilot study. Healthcare resource utilization during the 10 months prior to starting risperidone long acting will be retrospectively collected for all subjects (period A) at the beginning of the study. The utilization of direct medical resources will also be collected for 10 months after initiation of risperidone long acting (period B). In this design the patients will serve as their own control.

NCT ID: NCT00237874 Completed - Schizophrenia Clinical Trials

Aripiprazole Treatment of Prodromal Patients

Start date: February 2004
Phase: Phase 2/Phase 3
Study type: Interventional

We hypothesize that symptoms will improve in patients who meet diagnostic criteria for the schizophrenia prodrome when they are prescribed aripiprazole.

NCT ID: NCT00204087 Active, not recruiting - Schizophrenia Clinical Trials

Psychological Intervention for Persons in the Early Initial Prodromal State

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

The purpose of this randomized controlled trial is to develop a cognitive behavioral therapy (CBT) for persons with at risk mental states in the early initial prodromal state and to evaluate CBT in comparison to supportive counselling (SC).It is hypothesized that CBT is more effective than SC on transition to subthreshold psychosis, psychosis and schizophrenia as well as on prodromal symptoms and social adjustment.

NCT ID: NCT00203775 Terminated - Psychosis Clinical Trials

Haloperidol vs. Risperidone in the Treatment of Aggression in Psychotic Inmates

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

This study examines the efficacy of haldol versus risperdal in the treatment of aggression in psychotic prison inmates. It is hypothsized that risperdal will be more effective in decreasing aggression than haldol.