Pfizer/IVGTT/Ziprasidone/Olanzapine

• Status: Completed
• Trial end date: 2006-10-01
• Target enrollment: 0
• Participant gender: All

Summary

Abnormalities in peripheral glucose regulation and type 2 diabetes can occur more commonly in individuals with schizophrenia than in healthy subjects or in other psychiatric conditions. Antipsychotic treatment may contribute significantly to abnormalities in glucose regulation. Hyperglycemia can contribute to long-term cardiovascular disease risk that may already be increased in patients with schizophrenia due to higher rates of smoking, sedentary life style, obesity and under-treated hypertension and dyslipidemia. This project will characterize the effects on glucose control of the two most commonly prescribed newer antipsychotic medications, ziprasidone and olanzapine, in patients with schizophrenia.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Washington University School of Medicine
• Collaborator: Pfizer
• Treatments: Olanzapine; Ziprasidone

Criteria

Inclusion Criteria:

• Patients: meets DSM-IV criteria for schizophrenia, any type, or schizoaffective disorder;

• aged 18 to 60 years;

• able to give informed consent;

• no medication changes for 2 weeks prior to and during the period of study;

• Patients: currently taking an antipsychotic.

Exclusion Criteria:

• Controls: Axis I psychiatric disorder criteria met except for substance use disorders as below;

• meets DSM-IV criteria for the diagnoses of substance abuse or dependence within the past six months;

• involuntary legal status (as per Missouri law);

• the presence of any serious medical disorder that may (as confirmed by peer-reviewed literature) confound the assessment of symptoms, relevant biologic measures or diagnosis;

• the following conditions are currently identified:

• insulin- or non-insulin-dependent diabetes mellitus;

• any intra-abdominal or intrathoracic surgery or limb amputation within the prior 6 months;

• any diagnosed cardiac condition causing documented hemodynamic compromise;

• any diagnosed respiratory condition causing documented or clinically recognized hypoxia;

• pregnancy or high dose estrogens, fever, narcotic therapy, acute sedative hypnotic withdrawal, corticosteroid or spironolactone therapy, dehydration, epilepsy, endocrine disease, high-dose benzodiazepine therapy (> 25 mg/day of diazepam), or any medical condition known to interfere with glucose utilization;

• meets DSM-IV criteria for Mental Retardation (mild or worse).