TerminatedEUCTR 2010-019981-94
Attention Deficit Hyperactivity Disorder (ADHD) and opioid maintenance therapy. A randomized, placebo-controlled study of the efficacy of atomoxetine for treating adult ADHD in patients receiving o...
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Historical research recordFinland
Understand this study
What is this study about?
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
- Listed locations
- Finland
- 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 is historical registry information. What is the current study status and protocol?
Things to check before joining
Study start dateNot clearly listed
- Recruitment status
- Terminated
- Enrollment listed in the registry
- 30
- Sponsor
- HUS/ Neuropsykiatrian poliklinikka
- Sponsor type
- Unknown or unclear
- 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
- Finland
- Age range
- Not clearly listed
- Official registry ID
- EUCTR 2010-019981-94
- Official title
Show the full official title
Attention Deficit Hyperactivity Disorder (ADHD) and opioid maintenance therapy. A randomized, placebo-controlled study of the efficacy of atomoxetine for treating adult ADHD in patients receiving o...
Recruitment & locations
TerminatedThis badge reflects the study status reported by the registry. Check the registry for the latest information.
Finland
Registry details
Historical country statuses
- Finland — Prematurely Ended
Interested in joining this study?
Questions about this study
Who is behind this study?
The study sponsor is HUS/ Neuropsykiatrian poliklinikka.
Is this study still recruiting?
The historical registry lists this study as terminated.
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