Risperidone Treatment in Schizophrenia Patients Who Are Currently Taking Clozapine

NCT00056498 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 65

Last updated 2019-10-01

Study results available
· View outcomes & findings →

Summary

This study will determine whether adding the drug risperidone (Risperdal®) is more effective than placebo in treating schizophrenic patients who are taking the drug clozapine.

Conditions

Interventions

DRUG

Placebo

Placebo capsule daily for 16 weeks

DRUG

Risperdal

Risperdal 4 mg per day for 16 weeks

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • Ortho-McNeil Janssen Scientific Affairs, LLC

    collaborator INDUSTRY
  • University of Maryland, Baltimore

    lead OTHER

Principal Investigators

  • Robert W Buchanan, MD · University of Maryland, College Park

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-12-31
Primary Completion
2007-12-31
Completion
2007-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00056498 on ClinicalTrials.gov