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Risperidone Long-Acting for Alcohol and Schizophrenia Treatment (R-LAST)
The purpose of this study is to compare the efficacy of oral risperidone (Risperdal) to risperidone long-acting (Consta) in reducing alcohol use in persons diagnosed with schizophrenia or schizoaffective disorder.
Comorbid alcohol/substance use disorder (SUD) in people with schizophrenia is a major concern, both in view of the high frequency of SUD among patients with schizophrenia and the difficulty in managing such patients. Though antipsychotic medications are effective in reducing symptoms and impairment in persons with schizophrenia, the typical antipsychotic agents are of limited value in controlling alcohol/substance use in these patients. Extrapyramidal, dysphoric side effects of conventional neuroleptics may actually promote the use of substances in an attempt to counteract these effects. In addition, medication non-compliance is common among patients with schizophrenia. Novel antipsychotics have altered treatment expectations and outcomes for patients with severe forms of schizophrenia. A growing number of studies have assessed the effects of oral risperidone in persons with dual disorders. Potential mechanisms of action by which risperidone and other atypical antipsychotics could decrease substance use include being less likely to cause extrapyramidal side effects than typical agents, improving negative symptoms and ameliorating a dysfunction of the brain reward system. Risperidone long-acting injectable medication addresses issues of noncompliance, while avoiding peak blood levels of oral preparations, thereby minimizing EPS and improving negative symptoms of schizophrenia. Risperidone may also facilitate dopamine neurotransmission in the prefrontal cortex and correct a hypothesized dysfunction of the brain reward system. This study is an open, randomized, controlled study to compare intramuscular long-acting risperidone to oral risperidone with blinded ratings to determine whether the long-acting form of risperidone has greater efficacy in reducing substance use. Patients with schizophrenia or schizoaffective disorder, age 18 to 65, who are taking any single oral antipsychotic medication except clozapine or risperidone long-acting may be enrolled.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
JMH Mental Health Center, University of Miami
Miami, Florida, United States
School of Pharmacy, Univ. of Missouri Kansas City
Kansas City, Missouri, United States
Washington University School of Medicine
St Louis, Missouri, United States
West Central Behavioral Health
Lebanon, New Hampshire, United States
Mental Health Center of Greater Manchester
Manchester, New Hampshire, United States
Center for Psychiatric Advancement
Nashua, New Hampshire, United States
University of South Carolina
Columbia, South Carolina, United States
White River Junction Veterans Admininistration Medical Center
White River Junction, Vermont, United States
Start Date
September 1, 2005
Primary Completion Date
June 1, 2009
Completion Date
July 1, 2010
Last Updated
May 9, 2019
95
ACTUAL participants
Risperidone Long Acting
DRUG
oral risperidone
DRUG
Lead Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
NCT07455929
NCT07460453
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06740383