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NCT00607919 · ClinicalTrials.gov registry record · Phase 4

Treatment of ADHD With Atomoxetine in Children & Adolescents With ADHD & Comorbid Dyslexia

A Phase 4 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 4
Development phase
209
Enrollment target

NCT00607919: Completed Phase 4 study, sponsored by Eli Lilly and Company.

NCT00607919 is a Phase 4 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 209 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00607919, a Phase 4 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 4
Development phase
209 participants
Enrollment target

Study Summary

This study will evaluate the effect of atomoxetine in treating Attention-Deficit/Hyperactivity Disorder (ADHD) symptoms in children and adolescents with ADHD and comorbid reading disability (dyslexia)

Primary Outcome

Measures the 18 symptoms contained in the Diagnostic and Statistical Manual of Mental Disorders Fourth Edition, Text Revision (DSM-IV-TR) diagnosis of Attention-Deficit/Hyperactivity Disorder (ADHD). Individual item scores range from 0 (none/never or rarely) to 3 (severe/very often). Total scores range from 0-54. Least Square mean of change from baseline in ADHDRS is from a restricted maximum likelihood-based, mixed model repeated measures analysis which includes the effects of treatment, invest

Interventions

  • DRUG Placebo
  • DRUG Atomoxetine

Trial Details

FieldValue
Enrollment Target 209 participants
Start Date 2008-03
Est. Completion 2011-02
Phase Phase 4
Eli Lilly and Company

1,341 total trials

What the finished NCT00607919 record still lists

NCT00607919 is an interventional study that assigns participants to a tested intervention. The registered 209 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00607919 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00607919 about?

NCT00607919 is a clinical study titled "Treatment of ADHD With Atomoxetine in Children & Adolescents With ADHD & Comorbid Dyslexia". This study will evaluate the effect of atomoxetine in treating Attention-Deficit/Hyperactivity Disorder (ADHD) symptoms in children and adolescents with ADHD and comorbid reading disability (dyslexia)

What is the current status of trial NCT00607919?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 209 participants. The study started on 2008-03. Estimated completion is 2011-02.

What interventions are being tested in trial NCT00607919?

The interventions under investigation include: Placebo (DRUG), Atomoxetine (DRUG).

Who is sponsoring clinical trial NCT00607919?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00607919's enrollment target sits among peer trials

209 399th of 2000 higher than 1,602 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00607919, the US trial registry maintained by the National Library of Medicine. NCT00607919 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.