CompletedEUCTR 2005-004037-18
An Open Label, Multicentre Study to Evaluate the Long Term Safety of Prolonged Release (PR) OROS Methylphenidate (18, 36, 54, 72 and 90 mg/day) in Adults with Attention Deficit/Hyperactivity Disor...
This historical record does not confirm current site availability.
Historical research recordMultiple countriesADHD
Understand this study
What did researchers investigate?
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
- Germany · Portugal and 1 more location
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study information
Study start dateNot clearly listed
- Recruitment status
- Completed
- Enrollment listed in the registry
- 160
- Sponsor
- Janssen-Cilag Medical Affairs EMEA
- Sponsor type
- Unknown or unclear
- 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
- Germany, Portugal, Spain
- Age range
- Not clearly listed
- Official registry ID
- EUCTR 2005-004037-18
- Official title
Show the full official title
An Open Label, Multicentre Study to Evaluate the Long Term Safety of Prolonged Release (PR) OROS Methylphenidate (18, 36, 54, 72 and 90 mg/day) in Adults with Attention Deficit/Hyperactivity Disor...
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Explore recruiting studiesRecruitment & locations
CompletedGermany · Portugal · Spain
Questions about this study
Who is behind this study?
The study sponsor is Janssen-Cilag Medical Affairs EMEA.
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