drugset / Trial / NCT00114595

Ethyl-Eicosapentaenoic Acid and Tardive Dyskinesia

NCT00114595

RandomizedParallel-groupDouble-blindTreatment

Summary

Tardive dyskinesia is a common complication of conventional antipsychotic treatment in subjects with schizophrenia. This study investigates whether the addition of the omega-3 fatty acid, ethyl-eicosapentaenoic acid (EPA) to usual treatment improves movement disorder in 84 schizophrenia subjects with established tardive dyskinesia. The initial double-blinded, randomised trial duration is 12 weeks, followed by further 46 weeks of open-label treatment.

Timeline

Start
2003-04
Primary completion
Completion
2005-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Eicosapentaenoic acid Small molecule 2 g Oral