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TerminatedNCT00687609

Pilot Evaluation of Atomoxetine on Attention Deficit Hyperactivity Disorder (ADHD) Symptoms in Adolescents With Cannabis abusE

Medication studyAges 13–17Netherlands
The study in practice

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Who could participate?

This study is for people with ADHD. Listed age limits: 13 years to 17 years. Other eligibility criteria apply.

Listed locations
The HagueSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateSeptember 2008
Recruitment status
Terminated
Enrollment listed in the registry
7
Sponsor
Eli Lilly and Company
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
Netherlands
Age range
From 13 Years to 17 Years
Official registry ID
NCT00687609
Official title
Show the full official title

An Open Label Pilot Study of Atomoxetine Hydrochloride in Adolescents With Attention Deficit/Hyperactivity Disorder and Comorbid Cannabis Abuse.

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Recruitment & locations

Terminated

The Hague

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Eli Lilly and Company.

Does this study involve medication?

Yes. The study involves medication, including Atomoxetine.

Who can participate?

This study is for people with ADHD. Listed age limits: 13 years to 17 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as terminated.

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