drugset / Trial / NCT00231335

Efficacy and Safety Study of Escitalopram Augmentation in Treatment Resistant Schizophrenia

NCT00231335

Phase 4 Completed 30 enrolled Emory University Forest Laboratories · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

A primary hypothesis to be explored here is that, given its pharmacodynamic profile and hypothesized mechanisms associated with schizophrenia, escitalopram will, in comparison to placebo, be effective when added to risperidone or olanzapine treated group in reducing the severity of resistant symptoms, particularly existing subsyndromal anxiety and depression.

Timeline

Start
2006-03
Primary completion
Completion
2007-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Escitalopram Small molecule