Viewing Study NCT00216918


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Study NCT ID: NCT00216918
Status: COMPLETED
Last Update Posted: 2007-01-26
First Post: 2005-09-20
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Neuropsychological Functioning in Children With Attention-Deficit/Hyperactivity Disorder.
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: An Open-Label Pilot Study of Atomoxetine Hydrochloride to Evaluate Neuropsychological Function in Children Ages 6 to 10 Years With Attention-Deficit/Hyperactivity Disorder.
Status: COMPLETED
Status Verified Date: 2007-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the change in neuropsychological status from baseline to 6 months post-initiation of atomoxetine treatment in children ages 6 to 10.5 diagnosed with ADHD.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
B4Z-CA-S013 None None View