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Geodon for the Treatment of Refractory Social Anxiety Disorder — SAD  

Social Anxiety Disorder Clinical Trial

Official title:
Ziprasidone for the Treatment of Refractory Social Anxiety Disorder

Clinical Trial Summary

The purpose of this study is to examine the effectiveness and tolerability of augmentation treatment of ziprasidone to achieve remission among patients with social anxiety disorder (SAD) who did not remit on sertraline treatment alone

Clinical Trial Description

This is a two-phase study consisting of 8 weeks of open label treatment with sertraline (50-200 mg/day) in patients with SAD and in those who fail to demonstrate symptom remission on sertraline alone, 8 weeks of randomized, double-blind, placebo-controlled augmentation with ziprasidone. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00215150
Study type Interventional
Source Duke University
Contact
Status Completed
Phase Phase 2
Start date November 2004
Completion date July 2009
View Details
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