Trial | NCT00486798  Report issue

Title

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

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Terminated

  • Intervention/Treatment

    quetiapine ...

  • Study Participants

    None
The purpose of this study is to compare the efficacy of quetiapine IR, following rapid titration versus conventional titration in patients with acute psychosis
Study Started
May 31
2007
Primary Completion
Aug 31
2007
Study Completion
Aug 31
2007
Last Update
Dec 10
2010
Estimate

Drug Quetiapine

Procedure Rating Scales

Procedure Self Assessment Form

Procedure Blood and urine samples

Procedure Sleeping pattern

Criteria 

Inclusion Criteria:

provision of written informed consent
male or female, aged 18-65 years
requirement of hospitalization and in need for antipsychotic treatment for an acute psychotic episode
able to swallow tablets from Day 1

Exclusion Criteria:

In-patients who are anticipated to be discharged before evaluation of the primary outcome variable at Day 5
patients with known relevant clinical disease
history of syncope, or orthostatic hypotension
patients with known neutropenia
No Results Posted