Clinical Trials Directory

Trials / Completed

CompletedNCT01822730

A Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis

A Multiple-Center, Randomized, Double-Blind Study of Comparison of Paliperidone and Risperidone for Treatment of Patirnts With Methamphetamine-Associated Psychosis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Wei Hao · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGpaliperidonePaliperidone group,6mg/pill,6mg-12mg/day non-forced titration method,last 2-4weeks
DRUGRisperidoneRisperidone group,1mg/pill,2mg-6mg/day non-forced titration method,last 2-4weeks

Timeline

Start date
2013-02-01
Primary completion
2014-01-01
Completion
2014-05-01
First posted
2013-04-02
Last updated
2015-02-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01822730. Inclusion in this directory is not an endorsement.