A Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis
Primary Purpose
Methamphetamine Dependence
Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
paliperidone
Risperidone
Sponsored by
About this trial
This is an interventional treatment trial for Methamphetamine Dependence focused on measuring Methamphetamine-Associated Psychosis, Aripiprazole, Risperidone
Eligibility Criteria
Inclusion Criteria:
- Patients,Diagnostic and Statistical Manual of Mental Disorders 4thed. (DSM-IV) criteria for Methamphetamine-Associated Psychosis.
- Must sign a Information consent form.
- Required to provide detailed address and phone number
Exclusion Criteria:
- Serious organic disease.
- Suicide ideation or hurt others.
- Taking antipsychotic within two weeks before.
- drug allergy to Risperidone or paliperidone.
- pregnancy and breastfeeding women.
Sites / Locations
- The Second Xiangya Hospital of Central University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
paliperidone
.Risperidone
Arm Description
paliperidone arm,6mg/pill,6-12mg/day,non-forced titration method.last2-4weeks.
Risperidone arm and placebo tables,1mg/pill,2mg-6mg/day,non-forced titration method.last2-4weeks
Outcomes
Primary Outcome Measures
The severity of psychosis
Positive and Negative Syndrome Scale
Secondary Outcome Measures
Clinical general status
Clinical general rating scale
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01822730
Brief Title
A Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis
Official Title
A Multiple-Center, Randomized, Double-Blind Study of Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Wei Hao
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Methamphetamine-associated psychosis (MAP) has been considered a pharmacological or environmental pathogen model of schizophrenia (SCZ) due in part to similarities in clinical presentation (i.e. paranoia, hallucinations, disorganized speech, and negative symptoms), response to treatment (e.g.neuroleptics),and pathologic mechanisms (e.g. central dopaminergic neurotransmission) of both conditions. Both paliperidone and risperidone are second generation antipsychotics,but have same pharmacological effects of antipsychotic treatment and paliperidone may have more efficacy and safty.This study was designed to examine the acute efficacy, safety, and tolerability of paliperidone and risperidone for patients with MAP.
Detailed Description
Methods:A Multiple-Center, Randomized, Double-Blind.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Methamphetamine Dependence
Keywords
Methamphetamine-Associated Psychosis, Aripiprazole, Risperidone
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
paliperidone
Arm Type
Experimental
Arm Description
paliperidone arm,6mg/pill,6-12mg/day,non-forced titration method.last2-4weeks.
Arm Title
.Risperidone
Arm Type
Active Comparator
Arm Description
Risperidone arm and placebo tables,1mg/pill,2mg-6mg/day,non-forced titration method.last2-4weeks
Intervention Type
Drug
Intervention Name(s)
paliperidone
Other Intervention Name(s)
Paliperidone Extended-Release Tablets, Invega
Intervention Description
Paliperidone group,6mg/pill,6mg-12mg/day non-forced titration method,last 2-4weeks
Intervention Type
Drug
Intervention Name(s)
Risperidone
Other Intervention Name(s)
Risperdal H20070057
Intervention Description
Risperidone group,1mg/pill,2mg-6mg/day non-forced titration method,last 2-4weeks
Primary Outcome Measure Information:
Title
The severity of psychosis
Description
Positive and Negative Syndrome Scale
Time Frame
up to 4 weeks. participants will be followed for the duration of hospital stay
Secondary Outcome Measure Information:
Title
Clinical general status
Description
Clinical general rating scale
Time Frame
up to 4 weeks. participants will be followed for the duration of hospital stay
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients,Diagnostic and Statistical Manual of Mental Disorders 4thed. (DSM-IV) criteria for Methamphetamine-Associated Psychosis.
Must sign a Information consent form.
Required to provide detailed address and phone number
Exclusion Criteria:
Serious organic disease.
Suicide ideation or hurt others.
Taking antipsychotic within two weeks before.
drug allergy to Risperidone or paliperidone.
pregnancy and breastfeeding women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Hao, MD., Ph.D.
Organizational Affiliation
Central South University
Official's Role
Study Director
Facility Information:
Facility Name
The Second Xiangya Hospital of Central University
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410011
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
32296355
Citation
Wang G, Ding F, Chawarski MC, Hao W, Liu X, Deng Q, Ouyang X. Randomized Controlled Trial of Paliperidone Extended Release Versus Risperidone for the Treatment of Methamphetamine-Associated Psychosis in Chinese Patients. Front Psychiatry. 2020 Apr 1;11:237. doi: 10.3389/fpsyt.2020.00237. eCollection 2020.
Results Reference
derived
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A Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis
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