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CompletedEUCTR 2006-005674-47

Long-term efficacy and safety of agomelatine in non-depressed out-patients with Generalized Anxiety Disorder.A 26-week randomised double-blind placebo-controlled parallel group study following an ...

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 anxiety. Other eligibility criteria applied.

Listed locations
Denmark · Estonia and 3 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
500
Sponsor
Institut de Recherches Internationales Servier
Sponsor type
Research institute
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
Denmark, Estonia, Finland, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2006-005674-47
Official title
Show the full official title

Long-term efficacy and safety of agomelatine in non-depressed out-patients with Generalized Anxiety Disorder.A 26-week randomised double-blind placebo-controlled parallel group study following an ...

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Recruitment & locations

Completed

Denmark · Estonia · Finland

2 more locations
  • Hungary
  • Sweden
Registry details
Historical country statuses
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Institut de Recherches Internationales Servier, a research institute.

Who was this study for?

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

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