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Efficacy and Safety Study of Combination of Ginkgo Extract and Ginseng Extract in Children With ADHD(Attention Deficit Hyperactivity Disorder) — ADHD  

Mental Disorders Clinical Trial

Official title:
Randomized, Double-Blind, Placebo-control, Multicenter Study, the Efficacy and Safety of Combination of Ginkgo Extract and Ginseng Extract(YY-162)in Children With ADHD(Attention Deficit Hyperactivity Disorder)in 8 Weeks

Clinical Trial Summary

This study will evaluate clinical efficacy and safety of treatment with YY-162 in children with ADHD.

Clinical Trial Description

This is Double-Blind, two arms, multi-center, Interventional, 8 weeks study starting with YY-162(Combination of Ginkgo extract and Ginseng extract)in children with ADHD. Assessment of efficacy and safety will be performed at the baseline, weeks 2, 4 and 8. At the first visit, a full psychiatric history, demographic date and physical examination will be undertaken. Throughout the study, the following procedures, documentations and evaluations will performed; K-ARS, IOWA conner's rating scale, CGI-S/I, ATA, Children's color trails test and stroop test, intelligence test(from KEDI-WISC)and adverse event reporting. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01536210
Study type Interventional
Source Yuyu Pharma, Inc.
Contact
Status Completed
Phase Phase 3
Start date December 2011
Completion date December 2012
View Details
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