Overview

Risperidone and Olanzapine for the Schizophrenic Patients With Neuroleptic-Induced Tardive Dyskinesia

Status:
Completed
Trial end date:
2004-06-01
Target enrollment:
0
Participant gender:
All
Summary
We initiate a study with research grant from department of health and Taoyuan mental hospital and choose risperidone and olanzapine as study medications. We compare the effects of these 2 drugs in schizophrenic spectrum patients of Han ethnics with neuroleptic-induced tardive dyskinesia to test the hypothesis that these two medications have different effects in improving tardive dyskinesia.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Taoyuan Psychiatric Center, Ministry of Health and Welfare, Executive Yuan, R.O.C. Taiwan
Collaborator:
Department of Health
Treatments:
Antipsychotic Agents
Olanzapine
Risperidone
Criteria
Inclusion Criteria:

- Age of 18-70 y/o

- Female patients did not have pregnancy plans and must agree to use reliable pregnancy
prevention methods if during childbearing age

- Meet schizophrenia, schizophreniform or schizoaffective disorder criteria of DSM-IV

- Fulfill DSM-IV neuroleptic-induced tardive dyskinesia research criteria, the severity
of tardive dyskinesia was no less than moderate degree (> or =4) assessed by global
impression of Extrapyramidal System Rating Scale (item 42 of ESRS)

- Patients or legal responsible people agree to join study and sign informed consent

Exclusion Criteria:

- Had other axis I diagnosis of DSM-IV

- Unstable major systemic diseases

- Had neurological disorder influenced to EPS assessment

- Substance abuse or dependence other then coffee or tobacco within 6 months before
study