Effects of Atypical Versus Conventional Antipsychotics on the Prevalence of Tardive Dyskinesia
This study has been completed.
Sponsor:
Collaborator:
Yale University
Information provided by:
National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier:
NCT00237835
First received: October 7, 2005
Last updated: February 22, 2006
Last verified: October 2005
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Purpose
This study will compare the effects of newer atypical antipsychotics with those of older conventional antipsychotics on the risk of tardive dyskinesia.
| Condition |
|---|
|
Tardive Dyskinesia |
| Study Type: | Observational |
| Study Design: | Observational Model: Defined Population Observational Model: Natural History Time Perspective: Longitudinal Time Perspective: Prospective |
| Official Title: | Prevalence of Tardive Dyskinesia Among Patients Treated With Atypical Vs Conventional Antipsychotic |
Further study details as provided by National Institute of Mental Health (NIMH):
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- patients at the Connecticut Mental Health Center receving antipsychotics
Exclusion Criteria:
- severe neurological disease
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00237835 History of Changes |
| Other Study ID Numbers: | R01 MH61008, DSIR AT-SP |
| Study First Received: | October 7, 2005 |
| Last Updated: | February 22, 2006 |
| Health Authority: | United States: Federal Government |
Additional relevant MeSH terms:
|
Dyskinesias Movement Disorders Central Nervous System Diseases Nervous System Diseases Neurologic Manifestations Signs and Symptoms Antipsychotic Agents |
Tranquilizing Agents Central Nervous System Depressants Physiological Effects of Drugs Pharmacologic Actions Central Nervous System Agents Therapeutic Uses Psychotropic Drugs |
ClinicalTrials.gov processed this record on June 18, 2013