Viewing Study NCT00216918



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00216918
Status: COMPLETED
Last Update Posted: 2007-01-26
First Post: 2005-09-20

Brief Title: Neuropsychological Functioning in Children With Attention-DeficitHyperactivity Disorder
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

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-DeficitHyperactivity 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 105 diagnosed with ADHD
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
B4Z-CA-S013 None None None