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CompletedEUCTR 2012-002785-12

A 28-week, randomised, open-label study evaluating the effectiveness of aripiprazole once-monthly versus paliperidone palmitate in adult patients with schizophrenia

This historical record does not confirm current site availability.

Historical research recordMultiple countries
The study in practice

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.

Who was this study for?

This study was for people with schizophrenia. Other eligibility criteria applied.

Listed locations
Czechia · Estonia and 5 more locations
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
286
Sponsor
H. Lundbeck A/S
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
United Kingdom, Czechia, Estonia, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2012-002785-12
Official title
Show the full official title

A 28-week, randomised, open-label study evaluating the effectiveness of aripiprazole once-monthly versus paliperidone palmitate in adult patients with schizophrenia

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Recruitment & locations

Completed

Czechia · Estonia · Germany

4 more locations
  • Italy
  • Spain
  • Sweden
  • United Kingdom
Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is H. Lundbeck A/S.

Who was this study for?

This study was for people with schizophrenia. Other eligibility criteria applied.

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