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Clinical Trial Summary

The objective of this study is to evaluate predictors of response to antipsychotic medication in subjects with schizophrenia. The investigators will evaluate psychopathology,brain MRI, genetics and neuropsychological profile. Two groups of treatment will be compared: first generation antipsychotics vs. second generation antipsychotics. Participants will be randomized to one of the groups. Trial duration: 12 weeks.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01016145
Study type Interventional
Source University of Sao Paulo
Contact Monica Kayo, MD
Phone 551130696971
Email monica.kayo@usp.br
Status Recruiting
Phase Phase 4
Start date April 2009
Completion date July 2010

See also
  Status Clinical Trial Phase
Completed NCT02567370 - Single-ascending Dose Study With a Food-Effect Cohort to Evaluate AMG 581 Phase 1
Completed NCT02504476 - Multiple Ascending Dose Study on Safety, Tolerability, and Pharmacokinetics of AMG 581 in Healthy Subjects or Subjects With Schizophrenia or Schizoaffective Phase 1