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Clinical Trials/NCT00222807
NCT00222807
Completed
Not Applicable

Schizophrenia, Antipsychotic Treatment and the Risk for Diabetes Mellitus

University of Pittsburgh1 site in 1 country200 target enrollmentAugust 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
University of Pittsburgh
Enrollment
200
Locations
1
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This preliminary study aims to investigate the mechanism of higher rates of type 2 diabetes mellitus in patients with schizophrenia. As part of the study, we collect neuroendocrine-immune data on patients with first episode, treatment naive psychosis, patients with newly diagnosed schizophrenia and normal healthy controls.

Regardless the treatment status, we collect the same neuroendocrine-immune data on the participants after 2 months.

Detailed Description

This preliminary study aims to investigate the mechanism of higher rates of type 2 diabetes mellitus in patients with schizophrenia. As part of the study, we collect neuroendocrine-immune data on patients with first episode, treatment naive psychosis, patients with newly diagnosed schizophrenia and normal healthy controls. Regardless the treatment status, we collect the same neuroendocrine-immune on the participants (patients and controls) after 2 months. Thus, our study does not control treatment. Patients take treatment in consultation with their physician. Some of them even decide not to take any medications. At the 2nd visit, we do ask them about the the medications they are taking if any.

Registry
clinicaltrials.gov
Start Date
August 2003
End Date
March 2016
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Psychotic disorder as per DSM-IV criteria of the American Psychiatric Association

Exclusion Criteria

  • Diabetes, type 1 or 2
  • Prominent substance abuse (i.e. psychotic symptoms attributable entirely to substance use)
  • Age above 50 or age below 14

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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