Clinical Trials Directory

Trials / Completed

CompletedNCT00672373

Extract of Ginkgo Biloba and Tardive Dyskinesia

A Double-Blind, Randomised, Parallel-Group Comparison of Extract of Ginkgo Biloba(EGB-761) Versus Placebo as Add-on Medication in Patients With Established Tardive Dyskinesia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
157 (actual)
Sponsor
Beijing HuiLongGuan Hospital · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether Extract of Ginkgo Biloba is effective in the treatment on Tardive dyskinesia

Detailed description

Tardive dyskinesia(TD) is a common complication of conventional antipsychotic treatment in subjects with schizophrenia. There is no established treatment for TD patients.This disorder remains a significant clinical problem for both patients and physicians for the foreseeable future.

Conditions

Interventions

TypeNameDescription
DRUGExtract of Ginkgo Biloba (EGb-761 capsules)EGb-761 240mg/d, 1 capsule(80mg) tid,po,12 weeks; Each capsule contains 19.6mg flavonol glycosides and 4.8mg terpene lactones.
DRUGPlaceboWheat flour placebo capsule,1 capsule tid, po,12 weeks

Timeline

Start date
2006-12-01
Primary completion
2007-05-01
Completion
2007-08-01
First posted
2008-05-06
Last updated
2008-05-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00672373. Inclusion in this directory is not an endorsement.