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CompletedNCT00191659

Atomoxetine compared with usual care for quality of life in young people with ADHD

About this titleRead the official source — NCT00191659

This study evaluated the effectiveness of Atomoxetine Hydrochloride for people with ADHD.

Medication studyAges 7–15United Kingdom
The study in practice

Understand this study

What did researchers investigate?

This study evaluated the effectiveness of Atomoxetine Hydrochloride for people with ADHD.

Who was this study for?

This study was for people with ADHD. Listed age limits: 7 years to 15 years. Other eligibility criteria applied.

Listed locations
BasingstokeSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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Study clarity

Study information

Study start dateJune 2004
Recruitment status
Completed
Enrollment listed in the registry
200
Sponsor
Eli Lilly and Company
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United Kingdom
Age range
From 7 Years to 15 Years
Official registry ID
NCT00191659
Official title
Show the full official title

A Randomised, Controlled, Open-Label Study of the Broader Efficacy of Atomoxetine Hydrochloride in the Treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in Children and Adolescents

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Recruitment & locations

Completed

Basingstoke

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FAQ

Questions about this study

What did researchers investigate?

This study evaluated the effectiveness of Atomoxetine Hydrochloride for people with ADHD.

Who is behind this study?

The study sponsor is Eli Lilly and Company.

Did this study involve medication?

Yes. The study involved medication, including Atomoxetine Hydrochloride.

Who was this study for?

This study was for people with ADHD. Listed age limits: 7 years to 15 years. Other eligibility criteria applied.

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