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Fast Titration Of Quetiapine Versus Currently Approved Titration

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 3

Conditions

Psychotic Disorders

Treatments

Drug: Quetiapine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00254813
D1449L00003

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and tolerability of a more rapid dose titration in acute schizophrenic patients compared to the conventional titration.

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent, male or female between 18 and 60 years old, having acute exacerbation of their schizophrenia or schizoaffective disorder requiring admission to hospital. Should stay in hospital for at least 7 days.

Exclusion criteria

  • Patients treated with Risperdal consta or Clozapine last 28 days, pregnancy or breast-feeding, patients known to be intolerant or unresponsive to quetiapine, known arrhythmia, other serious medical conditions.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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