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N/A N=24 Randomized Treatment

Improving Diabetes Risk Factors in Persons With Schizophrenia or Bipolar Disorder by Switching to Ziprasidone

Schizophrenia · Schizoaffective Disorder · Bipolar Disorder

Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Nov 2012
Primary outcome: Primary: Insulin Sensitivity — 5.55; 1.88 mg glucose/kg.min/μIU insulin — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
ziprasidone (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
The University of Texas Health Science Center at San Antonio
Primary completion
Apr 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Insulin Sensitivity
6.01; 2.07
PRIMARY
Insulin Sensitivity
6.01; 2.07
SECONDARY
Body Mass Index
36.0; 38.8
SECONDARY
Body Mass Index
36.0; 38.8
SECONDARY
Abdominal Circumference
115; 122
SECONDARY
Abdominal Circumference
115; 122
SECONDARY
Systolic Blood Pressure
123; 128
SECONDARY
Systolic Blood Pressure
123; 128
SECONDARY
Diastolic Blood Pressure
82; 81
SECONDARY
Diastolic Blood Pressure
82; 81
SECONDARY
Triglycerides
154; 252
SECONDARY
Triglycerides
154; 252
SECONDARY
Cholesterol
177; 186
SECONDARY
Cholesterol
177; 186
SECONDARY
HDL Cholesterol
40; 38
SECONDARY
HDL Cholesterol
40; 38
SECONDARY
LDL Cholesterol
106; 109
SECONDARY
LDL Cholesterol
106; 109

Summary

Having a diagnosis of schizophrenia or bipolar disorder and being treated with certain of the newer antipsychotics are risk factors for development of diabetes. Subjects with these risk factors plus obesity and/or family history of diabetes who agree to study participation will undergo an oral glucose tolerance test. If the oral glucose tolerance test demonstrates that the subject is pre-diabetic (elevated glucose levels, but below the diabetic range), he/she will have his/her insulin resistance level measured, prior to random assignment to either stay on current antipsychotic medication or switch to ziprasidone. Insulin resistance will be measured again after four months. The primary hypothesis is that insulin resistance will decrease in those switched to ziprasidone relative to those continuing on their same antipsychotic medication.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of schizophrenia or schizoaffective disorder or bipolar disorder
  • BMI>29.9 or family history of diabetes and/or abdominal circumference greater than 88 cm in women or 102 cm in men
  • Pre-diabetic oral glucose tolerance test
  • Current treatment with olanzapine, risperidone, paliperidone, or quetiapine, or combination of these
  • Willing to switch to ziprasidone
  • No psychiatric hospitalizations in past three months and judged by treating clinician to be suitable for antipsychotic medication switch
  • Able to give informed consent to study

Exclusion Criteria

  • Judged to be currently suicidal, homicidal, or unable to cooperate with treatment
  • Unstable serious medical illness
  • Current use of drugs that interfere with glucose and fat metabolism (sulfonylureas, metformin, thiazolidinediones). The use of "statins" and fibrates will be allowed ONLY if stable dose for past 3 months.
  • Current diagnosis of diabetes
  • Fasting blood glucose >125 mg/dl
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00538642). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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