search
Back to results

Risperidone Long-acting Versus Oral Risperidone in Patients With Schizophrenia and Alcohol Use Disorder

Primary Purpose

Schizophrenia, Psychotic Disorders, Substance Abuse

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Risperidone Long Acting
oral risperidone
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Risperidone, Schizophrenia, Substance Use Disorder, Alcohol Use Disorder, Treatment, Schizoaffective Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ages 18-65 Schizophrenia or schizoaffective disorder Meets the Structured Clinical Interview for DSM-IV (SCID) criteria for an alcohol use disorder Alcohol use on at least 5 days during the 4 weeks prior to randomization Patient is medically stable to start either form of risperidone. Exclusion Criteria: Current treatment with clozapine. Current treatment with injectable risperidone long-acting. Currently pregnant, planning to become pregnant, or unwilling to use an acceptable form of birth control. Change in medications (dose of current medication, discontinuation of medication, or new medication) in past 30 days. History of or current breast cancer. History of intolerance of or allergy to risperidone or risperidone long-acting. Currently residing in a residential program designed to treat substance use disorders. Current treatment with long-acting, injectable antipsychotic medication will require a review by the medication adjustment group before entering the client into the study. Past treatment with risperidone long-acting will require a review by the medication adjustment group before entering the client into the study. Treatment at baseline with a second antipsychotic medication will require a review by the medication adjustment group before entering the client into the study. Treatment at baseline with a psychotropic agent proposed to curtail substance use will require a review by the medication adjustment group before entering the client into the study. Patients who, in the opinion of the investigator, are judged unsuitable to participate in the study.

Sites / Locations

  • JMH Mental Health Center, University of Miami
  • School of Pharmacy, Univ. of Missouri Kansas City
  • Washington University School of Medicine
  • West Central Behavioral Health
  • Mental Health Center of Greater Manchester
  • Center for Psychiatric Advancement
  • University of South Carolina
  • White River Junction Veterans Admininistration Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Risperidone Long Acting

Oral Risperidone

Arm Description

Risperidone Long Acting; aka Risperdal Consta; injectable form

Oral Risperidone; aka Risperdal; oral form

Outcomes

Primary Outcome Measures

Change Over Time in Frequency of Heavy Drinking Days (Used to Evaluate Treatment Efficacy)
Frequency of heavy drinking days is obtained each week retrospectively as the number of heavy drinking days during the prior week (assessed by the Timeline Followback Scale). A heavy drinking day is defined as 4 or more drinks per day for a female and 5 or more drinks per day for a male. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.

Secondary Outcome Measures

Average Over Time of Frequency of Drinking Days (Used to Evaluate Treatment Efficacy)
Frequency of drinking days is obtained each week retrospectively as the number of drinking days during the prior week (assessed using the Timeline Followback). Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Average Over Time of Severity of Illness and Global Improvement (Used to Evaluate Treatment Efficacy)
A rater assesses the severity of illness and global impression using a scale from 1 to 7 (Clinical Global Impression), where higher values represent a worse outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Average Over Time of Positive and Negative Symptoms (Used to Evaluate Treatment Efficacy)
A rater assesses positive and negative symptoms of schizophrenia using a 30-item scale (Positive and Negative Symptom Score) Scores range from 30 to 210, where higher values represent a worse outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Average Over Time of Global Functioning (Used to Evaluate Treatment Efficacy)
A rater assesses social, occupational and psychological functioning on a hypothetical continuum of mental health - illness (using Global Assessment of Functioning); scores range from 100 to 1, where higher values represent a better outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Number of Participants With Medication Adherence
Number of participants with medication adherence (defined as taking medication at least 75% of the days in the treatment period).

Full Information

First Posted
August 15, 2005
Last Updated
April 16, 2019
Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
Janssen, LP
search

1. Study Identification

Unique Protocol Identification Number
NCT00130923
Brief Title
Risperidone Long-acting Versus Oral Risperidone in Patients With Schizophrenia and Alcohol Use Disorder
Official Title
Risperidone Long-Acting for Alcohol and Schizophrenia Treatment (R-LAST)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
July 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
Janssen, LP

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Psychotic Disorders, Substance Abuse, Alcohol Abuse
Keywords
Risperidone, Schizophrenia, Substance Use Disorder, Alcohol Use Disorder, Treatment, Schizoaffective Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
95 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Risperidone Long Acting
Arm Type
Experimental
Arm Description
Risperidone Long Acting; aka Risperdal Consta; injectable form
Arm Title
Oral Risperidone
Arm Type
Active Comparator
Arm Description
Oral Risperidone; aka Risperdal; oral form
Intervention Type
Drug
Intervention Name(s)
Risperidone Long Acting
Other Intervention Name(s)
Risperdal Consta
Intervention Description
Dose 25.00, 37.50 or 50.00 mg q two weeks
Intervention Type
Drug
Intervention Name(s)
oral risperidone
Other Intervention Name(s)
Risperdal
Intervention Description
0.50-6.00 mg oral risperidone daily
Primary Outcome Measure Information:
Title
Change Over Time in Frequency of Heavy Drinking Days (Used to Evaluate Treatment Efficacy)
Description
Frequency of heavy drinking days is obtained each week retrospectively as the number of heavy drinking days during the prior week (assessed by the Timeline Followback Scale). A heavy drinking day is defined as 4 or more drinks per day for a female and 5 or more drinks per day for a male. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Average Over Time of Frequency of Drinking Days (Used to Evaluate Treatment Efficacy)
Description
Frequency of drinking days is obtained each week retrospectively as the number of drinking days during the prior week (assessed using the Timeline Followback). Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Time Frame
6 months
Title
Average Over Time of Severity of Illness and Global Improvement (Used to Evaluate Treatment Efficacy)
Description
A rater assesses the severity of illness and global impression using a scale from 1 to 7 (Clinical Global Impression), where higher values represent a worse outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Time Frame
6 months
Title
Average Over Time of Positive and Negative Symptoms (Used to Evaluate Treatment Efficacy)
Description
A rater assesses positive and negative symptoms of schizophrenia using a 30-item scale (Positive and Negative Symptom Score) Scores range from 30 to 210, where higher values represent a worse outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Time Frame
6 months
Title
Average Over Time of Global Functioning (Used to Evaluate Treatment Efficacy)
Description
A rater assesses social, occupational and psychological functioning on a hypothetical continuum of mental health - illness (using Global Assessment of Functioning); scores range from 100 to 1, where higher values represent a better outcome. Mixed models are used to obtain estimates of efficacy from the partial data provided by each subject while adherent to assigned treatment (under the 'missing at random' assumption). The 'explanatory' estimands (target of the mixed model estimation) are defined in terms of population quantities that would have occurred had all subjects remained on assigned treatment throughout the study. The point estimate for each arm is reported under Number.
Time Frame
6 months
Title
Number of Participants With Medication Adherence
Description
Number of participants with medication adherence (defined as taking medication at least 75% of the days in the treatment period).
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 18-65 Schizophrenia or schizoaffective disorder Meets the Structured Clinical Interview for DSM-IV (SCID) criteria for an alcohol use disorder Alcohol use on at least 5 days during the 4 weeks prior to randomization Patient is medically stable to start either form of risperidone. Exclusion Criteria: Current treatment with clozapine. Current treatment with injectable risperidone long-acting. Currently pregnant, planning to become pregnant, or unwilling to use an acceptable form of birth control. Change in medications (dose of current medication, discontinuation of medication, or new medication) in past 30 days. History of or current breast cancer. History of intolerance of or allergy to risperidone or risperidone long-acting. Currently residing in a residential program designed to treat substance use disorders. Current treatment with long-acting, injectable antipsychotic medication will require a review by the medication adjustment group before entering the client into the study. Past treatment with risperidone long-acting will require a review by the medication adjustment group before entering the client into the study. Treatment at baseline with a second antipsychotic medication will require a review by the medication adjustment group before entering the client into the study. Treatment at baseline with a psychotropic agent proposed to curtail substance use will require a review by the medication adjustment group before entering the client into the study. Patients who, in the opinion of the investigator, are judged unsuitable to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan I. Green, MD
Organizational Affiliation
Dartmouth Medical School, Dartmouth College
Official's Role
Principal Investigator
Facility Information:
Facility Name
JMH Mental Health Center, University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
School of Pharmacy, Univ. of Missouri Kansas City
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
West Central Behavioral Health
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03766
Country
United States
Facility Name
Mental Health Center of Greater Manchester
City
Manchester
State/Province
New Hampshire
ZIP/Postal Code
03101
Country
United States
Facility Name
Center for Psychiatric Advancement
City
Nashua
State/Province
New Hampshire
ZIP/Postal Code
03060
Country
United States
Facility Name
University of South Carolina
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29203
Country
United States
Facility Name
White River Junction Veterans Admininistration Medical Center
City
White River Junction
State/Province
Vermont
ZIP/Postal Code
05009
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
8166327
Citation
Albanese MJ, Khantzian EJ, Murphy SL, Green AI. Decreased substance use in chronically psychotic patients treated with clozapine. Am J Psychiatry. 1994 May;151(5):780-1. doi: 10.1176/ajp.151.5.780b. No abstract available.
Results Reference
background
Citation
Albanese M. Risperidone in substance abusers with bipolar disorder. Presented at the 39th Annual Meeting of the American College of Neuropsychopharmacology. Sa Juan, PR, 2000.
Results Reference
background
Citation
Akaike, H, Information theory and an extension of the maximum likelihood principle., in 2nd International Symposium on Information Theory and Control., EBN Petrovand & C. Csaki, Editors. 1973, Akademia Kiado: Budapest, p. 267-281.
Results Reference
background
PubMed Identifier
8473874
Citation
Bartels SJ, Teague GB, Drake RE, Clark RE, Bush PW, Noordsy DL. Substance abuse in schizophrenia: service utilization and costs. J Nerv Ment Dis. 1993 Apr;181(4):227-32. doi: 10.1097/00005053-199304000-00003.
Results Reference
background
PubMed Identifier
7701146
Citation
Birkett MA, Day SJ. Internal pilot studies for estimating sample size. Stat Med. 1994 Dec 15-30;13(23-24):2455-63. doi: 10.1002/sim.4780132309.
Results Reference
background
PubMed Identifier
1970670
Citation
Bowers MB Jr, Mazure CM, Nelson JC, Jatlow PI. Psychotogenic drug use and neuroleptic response. Schizophr Bull. 1990;16(1):81-5. doi: 10.1093/schbul/16.1.81.
Results Reference
background
PubMed Identifier
8109646
Citation
Buckley P, Thompson P, Way L, Meltzer HY. Substance abuse among patients with treatment-resistant schizophrenia: characteristics and implications for clozapine therapy. Am J Psychiatry. 1994 Mar;151(3):385-9. doi: 10.1176/ajp.151.3.385.
Results Reference
background
PubMed Identifier
7961553
Citation
Buckley P, Thompson PA, Way L, Meltzer HY. Substance abuse and clozapine treatment. J Clin Psychiatry. 1994 Sep;55 Suppl B:114-6.
Results Reference
background
PubMed Identifier
9561949
Citation
Buckley PF. Novel antipsychotic medications and the treatment of comorbid substance abuse in schizophrenia. J Subst Abuse Treat. 1998 Mar-Apr;15(2):113-6. doi: 10.1016/s0740-5472(97)00134-7.
Results Reference
background
PubMed Identifier
9541335
Citation
Buckley PF. Substance abuse in schizophrenia: a review. J Clin Psychiatry. 1998;59 Suppl 3:26-30.
Results Reference
background
PubMed Identifier
10538860
Citation
Buckley PF, Miller A, Chiles JA, Sajatovic M. Implementing effectiveness research and improving care for schizophrenia in real-world settings. Am J Manag Care. 1999 Jun 25;5 Spec No:SP47-56.
Results Reference
background
Citation
Buckley P, McCarthy M, Chapman P, Richman C, Yamamoto B. Clozapine treatment of comorbid substance abuse in patients with schizophrenia. Schizophr Res 1999, 36:272.
Results Reference
background
PubMed Identifier
12225495
Citation
Coldham EL, Addington J, Addington D. Medication adherence of individuals with a first episode of psychosis. Acta Psychiatr Scand. 2002 Oct;106(4):286-90. doi: 10.1034/j.1600-0447.2002.02437.x.
Results Reference
background
PubMed Identifier
10885642
Citation
Drake RE, Xie H, McHugo GJ, Green AI. The effects of clozapine on alcohol and drug use disorders among patients with schizophrenia. Schizophr Bull. 2000;26(2):441-9. doi: 10.1093/oxfordjournals.schbul.a033464.
Results Reference
background
PubMed Identifier
1485053
Citation
Frison L, Pocock SJ. Repeated measures in clinical trials: analysis using mean summary statistics and its implications for design. Stat Med. 1992 Sep 30;11(13):1685-704. doi: 10.1002/sim.4780111304.
Results Reference
background
PubMed Identifier
10370435
Citation
Green AI, Zimmet SV, Strous RD, Schildkraut JJ. Clozapine for comorbid substance use disorder and schizophrenia: do patients with schizophrenia have a reward-deficiency syndrome that can be ameliorated by clozapine? Harv Rev Psychiatry. 1999 Mar-Apr;6(6):287-96. doi: 10.3109/10673229909017206.
Results Reference
background
PubMed Identifier
12769622
Citation
Green AI, Salomon MS, Brenner MJ, Rawlins K. Treatment of schizophrenia and comorbid substance use disorder. Curr Drug Targets CNS Neurol Disord. 2002 Apr;1(2):129-39. doi: 10.2174/1568007024606230.
Results Reference
background
PubMed Identifier
12505141
Citation
Green AI, Burgess ES, Dawson R, Zimmet SV, Strous RD. Alcohol and cannabis use in schizophrenia: effects of clozapine vs. risperidone. Schizophr Res. 2003 Mar 1;60(1):81-5. doi: 10.1016/s0920-9964(02)00231-1.
Results Reference
background
PubMed Identifier
11950550
Citation
Hunt GE, Bergen J, Bashir M. Medication compliance and comorbid substance abuse in schizophrenia: impact on community survival 4 years after a relapse. Schizophr Res. 2002 Apr 1;54(3):253-64. doi: 10.1016/s0920-9964(01)00261-4.
Results Reference
background
PubMed Identifier
3904487
Citation
Khantzian EJ. The self-medication hypothesis of addictive disorders: focus on heroin and cocaine dependence. Am J Psychiatry. 1985 Nov;142(11):1259-64. doi: 10.1176/ajp.142.11.1259.
Results Reference
background
PubMed Identifier
9385000
Citation
Khantzian EJ. The self-medication hypothesis of substance use disorders: a reconsideration and recent applications. Harv Rev Psychiatry. 1997 Jan-Feb;4(5):231-44. doi: 10.3109/10673229709030550.
Results Reference
background
PubMed Identifier
12416599
Citation
Lacro JP, Dunn LB, Dolder CR, Leckband SG, Jeste DV. Prevalence of and risk factors for medication nonadherence in patients with schizophrenia: a comprehensive review of recent literature. J Clin Psychiatry. 2002 Oct;63(10):892-909. doi: 10.4088/jcp.v63n1007.
Results Reference
background
PubMed Identifier
7168798
Citation
Laird NM, Ware JH. Random-effects models for longitudinal data. Biometrics. 1982 Dec;38(4):963-74.
Results Reference
background
Citation
Lee, ET. Statistical Methods for Survival Analysis. 1992, New York: John Wiley & Sons.
Results Reference
background
PubMed Identifier
11440773
Citation
Newton TF, Ling W, Kalechstein AD, Uslaner J, Tervo K. Risperidone pre-treatment reduces the euphoric effects of experimentally administered cocaine. Psychiatry Res. 2001 Jul 24;102(3):227-33. doi: 10.1016/s0165-1781(01)00255-4.
Results Reference
background
PubMed Identifier
11278158
Citation
Salyers MP, Mueser KT. Social functioning, psychopathology, and medication side effects in relation to substance use and abuse in schizophrenia. Schizophr Res. 2001 Mar 1;48(1):109-23. doi: 10.1016/s0920-9964(00)00063-3.
Results Reference
background
PubMed Identifier
1970669
Citation
Siris SG. Pharmacological treatment of substance-abusing schizophrenic patients. Schizophr Bull. 1990;16(1):111-22. doi: 10.1093/schbul/16.1.111.
Results Reference
background
PubMed Identifier
12355680
Citation
Smelson DA, Losonczy MF, Davis CW, Kaune M, Williams J, Ziedonis D. Risperidone decreases craving and relapses in individuals with schizophrenia and cocaine dependence. Can J Psychiatry. 2002 Sep;47(7):671-5. doi: 10.1177/070674370204700710.
Results Reference
background
Citation
Tukey, JW. Exploratory Data Analysis. 1977, Reading, MA: Addison Wesley Publ. Co.
Results Reference
background
Citation
Waternaux, C, Laird, N, Ware, J. Methods for the analysis of longitudinal data: Blood concentrations and cognitive development. J.Amer. Stat. Assoc. 1989: 84, p.33-41.
Results Reference
background
PubMed Identifier
1557567
Citation
Weiss RE, Lazaro CG. Residual plots for repeated measures. Stat Med. 1992 Jan 15;11(1):115-24. doi: 10.1002/sim.4780110110.
Results Reference
background
PubMed Identifier
10653215
Citation
Zimmet SV, Strous RD, Burgess ES, Kohnstamm S, Green AI. Effects of clozapine on substance use in patients with schizophrenia and schizoaffective disorder: a retrospective survey. J Clin Psychopharmacol. 2000 Feb;20(1):94-8. doi: 10.1097/00004714-200002000-00016.
Results Reference
background
PubMed Identifier
26302441
Citation
Green AI, Brunette MF, Dawson R, Buckley P, Wallace AE, Hafez H, Herz M, Narasimhan M, Noordsy DL, O'Keefe C, Sommi RW, Steinbook RM, Weeks M. Long-acting injectable vs oral risperidone for schizophrenia and co-occurring alcohol use disorder: a randomized trial. J Clin Psychiatry. 2015 Oct;76(10):1359-65. doi: 10.4088/JCP.13m08838.
Results Reference
derived

Learn more about this trial

Risperidone Long-acting Versus Oral Risperidone in Patients With Schizophrenia and Alcohol Use Disorder

We'll reach out to this number within 24 hrs