Overview

Risperidone and Olanzapine for the Schizophrenic Patients With Neuroleptic-Induced Acute Dystonia or Parkinsonism

Status:
Completed
Trial end date:
2003-07-01
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 incidence of using anticholinergic drugs in schizophrenic patients of Han ethnics with neuroleptic-induced acute dystonia or parkinsonism to test the hypothesis that these two medications have different EPS incidence in EPS intolerant population.
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 18-65 y/o;

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

- Meet schizophrenia criteria of DSM-IV;

- Fulfill DSM-IV neuroleptic-induced acute dystonia or parkinsonism research criteria,
the severity of acute dystonia or parkinsonism was greater than moderate degree (>4)
assessed by global impression of Extrapyramidal System Rating Scale (item 43 and 44 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