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Clinical Trials/NCT00569764
NCT00569764UnknownNot Applicable

The Effects of Metabolic Parameters of Aripiprazole in Patients With Schizophrenia

Seoul National Hospital1 site in 1 country100 target enrollmentStarted: December 2007Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
weight lipid profile : HDL, LDL, total-cholesterol, triglyceride fasting blood glucose

Study Overview

Brief Summary

To measure the long-term changes in weight and plasma lipids after switching antipsychotic treatment to aripiprazole

Detailed Description

To measure the long-term changes in weight, plasma lipids and fasting blood glucose after switching antipsychotic treatment to aripiprazole, 1 year, open label studies in out and in-patients with schizophrenia.

The measurement of weight and lipid profile and fasting blood glucose will be measured at baseline and every 3 months for 1 year.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • DSM-IV diagnosis with schizophrenia
  • who signed an informed consent

Exclusion Criteria

  • comorbid with substance abuse or substance dependence
  • pregnancy or lactation

Outcomes

Primary Outcomes

weight lipid profile : HDL, LDL, total-cholesterol, triglyceride fasting blood glucose

Time Frame: 1 year

Secondary Outcomes

  • prolactin ECG(1 year)

Investigators

Sponsor
Seoul National Hospital
Sponsor Class
Other Gov

Study Sites (1)

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