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Quetiapine Vs Haloperidol Decanoate for the Long Term Treatment of Schizophrenia and Schizoaffective Disorder
This study has been completed.
Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00018642
  Purpose

The purpose of this research study is to determine whether a new drug for schizophrenia is better for the maintenance treatment than a standard drugs currently prescribed. The new medication is called quetiapine and it will be compared with a standard medication called haloperidol decanoate. The study will determine if quetiapine causes fewer problems than haloperidol with side effects such as stiffness and restlessness and whether it costs the VA more or less to treat patients with quetiapine. In addition, blood samples will be collected every three months to determine if certain chemicals in the blood can influence the outcome of the subjects' illness.


Condition Intervention
Schizophrenia
Schizoaffective Disorder
Drug: quetiapine
Drug: haloperidol decanoate

MedlinePlus related topics: Schizophrenia
Drug Information available for: Quetiapine Quetiapine fumarate Haloperidol Haloperidol decanoate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Uncontrolled, Parallel Assignment, Efficacy Study
Official Title: Predicting the Optimal Pharmacotherapy for Outpatients With Schizophrenia

Further study details as provided by Department of Veterans Affairs:

Study Start Date: April 1997
Estimated Study Completion Date: March 2002
  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria

  1. Schizophrenia or Schizoaffective Disorder diagnosed by DSM-IV
  2. Between the ages 18-60.
  3. A candidate for maintenance antipsychotic therapy. This means that patients will have had at least two documented episodes of acute schizophrenic illness or at least two years of continuing psychotic symptoms.

Exclusion Criteria

  1. Organic brain disease.
  2. Mental Retardation
  3. Chronic medical illness which would make antipsychotic medication inappropriate.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00018642

Locations
United States, California
VA Greater Los Angeles Healthcare System
Los Angeles, California, United States, 90073
Sponsors and Collaborators
  More Information

Study ID Numbers: MHBS-042-96F
Study First Received: July 3, 2001
Last Updated: June 23, 2005
ClinicalTrials.gov Identifier: NCT00018642  
Health Authority: United States: Federal Government

Keywords provided by Department of Veterans Affairs:
quetiapine
haloperidol decanoate

Study placed in the following topic categories:
Haloperidol
Schizophrenia
Haloperidol decanoate
Quetiapine
Dopamine
Mental Disorders
Psychotic Disorders
Schizophrenia and Disorders with Psychotic Features

Additional relevant MeSH terms:
Neurotransmitter Agents
Disease
Tranquilizing Agents
Molecular Mechanisms of Pharmacological Action
Anti-Dyskinesia Agents
Physiological Effects of Drugs
Gastrointestinal Agents
Psychotropic Drugs
Central Nervous System Depressants
Antiemetics
Dopamine Antagonists
Antipsychotic Agents
Pharmacologic Actions
Pathologic Processes
Autonomic Agents
Therapeutic Uses
Dopamine Agents
Peripheral Nervous System Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on January 16, 2009