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TerminatedNCT00486798

FAST-A Study to Evaluate the Efficacy and Safety of Quetiapin IR in Patients With Acute Psychosis

Medication studyAges 18–65SwedenSchizophrenia
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 65 years.

Listed locations
Borås and 12 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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 dateMay 2007
Recruitment status
Terminated
Enrollment listed in the registry
Not clearly listed
Sponsor
AstraZeneca
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug, PROCEDURE
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Sweden
Age range
From 18 Years to 65 Years
Official registry ID
NCT00486798
Official title
Show the full official title

FAST-A Study to Evaluate the Efficacy and Safety of Quetiapin IR in Patients With Acute Psychosis

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Recruitment & locations

Terminated

Borås · Danderyd · Falköping

10 more locations
  • Gothenburg
  • Karlskrona
  • Malmö
  • Öjebyn
  • Piteå
  • Simrishamn
  • Stockholm
  • Trollhättan
  • Vaxjo
  • Västerås

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is AstraZeneca.

Does this study involve medication?

Yes. The study involves medication, including Quetiapine.

Who can participate?

Listed age limits: 18 years to 65 years.

Is this study still recruiting?

The registry lists this study as terminated.

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