Schizophrenia Clinical Trial
Official title:
Efficacy of Quetiapine in Treating Patients With Active Substance Use Disorder and Schizophrenia
Verified date | March 2018 |
Source | Dartmouth-Hitchcock Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to examine the efficacy of quetiapine (Seroquel) in reducing substance use in persons diagnosed with schizophrenia. The primary hypothesis is that quetiapine treatment will be associated with a decrease in substance use.
Status | Completed |
Enrollment | 23 |
Est. completion date | October 2008 |
Est. primary completion date | September 2006 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Age 18-65 - Schizophrenia or schizoaffective disorder - Meets Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (SCID) criteria for a substance use disorder (alcohol use disorder [AUD]; abuse or dependence) - Active substance use on at least 8 days during the 4 weeks prior to randomization. - Current treatment with antipsychotic medication. - Able to provide informed consent, or in the case of patients with legal court appointed guardians willing to give assent, with the consent of the guardian. - Not actively suicidal. Exclusion Criteria: - Current treatment with, decanoate antipsychotic, clozapine, or doses of quetiapine not approved by the team of investigators. Individuals treated with depot antipsychotic must wait until the end of their injection cycle before starting on study medication. - Currently pregnant, planning to become pregnant, or unwilling to use an acceptable form of birth control. - Currently residing in a residential program designed to treat substance use disorders. - Treatment at baseline with a psychotropic agent proposed to curtail substance use. - Patients who, in the opinion of the investigator, are judged unsuitable to participate in the study. - Unable to take part in the assessments in a meaningful way - Hypersensitivity/intolerance to quetiapine - Serious, unstable medical condition - Participation in clinical trial of an investigational drug within 30 days of baseline visit, or concurrent participation in a treatment study of a psychosocial intervention |
Country | Name | City | State |
---|---|---|---|
United States | Medical College of Georgia | Augusta | Georgia |
United States | Dartmouth-Hitchcock Medical Center | Lebanon | New Hampshire |
United States | West Central Behavioral Health | Lebanon | New Hampshire |
United States | Mental Health Center of Greater Manchester | Manchester | New Hampshire |
Lead Sponsor | Collaborator |
---|---|
Dartmouth-Hitchcock Medical Center | AstraZeneca, Augusta University |
United States,
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* Note: There are 26 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean Number of Drinking Days Per Week | Timeline Follow-back (TLFB) procedure was used at screening and baseline to establish current substance use, and it was also used weekly during the course of the study to assess continued alcohol and other substance use. TLFB cosisted of using a calendar and sasking participants to report alcohol and other drug use since last visit. At the screening visit, the TLFB was done for the four weeks prior to the visit. | 12 Weeks | |
Secondary | Clinical Symptoms | The main outcome measure of clinical symptoms was the Positive and Negative Symptoms Scale. This is a 30 item scale for assessing patients diagnosed with schizophrenia. Each item is rated on a 1 (absent) to 7 (extreme) scale. The minimum total score is 30 and the maximum is 210. | 12 Weeks |
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