University of Massachusetts Medical School
Worcester, Massachusetts, 01605, United States
NCT Number: NCT00981526
This is a 12-week, randomized, double-blinded, placebo-controlled trial of telmisartan 80 mg/day as an adjunctive to clozapine or olanzapine therapy, in 70 schizophrenia subjects to examine telmisartan's effect on glucose metabolism, weight, food intake, resting energy expenditure, and body composition. In addition, the study will examine insulin's effects on psychopathology and cognition.
Potential subjects will be identified by their clinicians at the Freedom Trail Clinic, or Massachusetts General Hospital. Approximately 70 subjects will be enrolled.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 4
Worcester, Massachusetts, 01605, United States
The specific aims include:
Primary Aims:
Secondary Aims:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Telmisartan 40mg/day for the first 2 weeks.
Telmisartan 80mg/day for the next 10 weeks.
Placebo (plus existing clozapine or olanzapine treatment) for 12 weeks.
Clozapine (plus telmisartan or placebo) for 12 weeks.
Olanzapine (plus telmisartan or placebo) for 12 weeks.
Time frame: 12 weeks
Insulin resistance as estimated by homeostasis model of assessment of insulin resistance (HOMA-IR) at week 12 in both the experimental and placebo arm. Insulin resistance is a condition in which cells fail to respond to the normal action of the hormone in the body. The HOMA-IR is calculated using a subject's fasting plasma insulin and glucose levels. The higher the score, the higher the level of insulin resistance.
Time frame: 12 weeks
Fasting triglycerides assessed in both experimental and placebo arm at week 12.
Time frame: 12 weeks
Lipid metabolism - fasting low density lipoprotein (LDL) and high density lipoprotein (HDL) are estimated in both experimental and placebo arms at 12 weeks.
Time frame: 12 weeks
The Positive and Negative Syndrome Scale (PANSS) and Scale for the Assessment of Negative Symptoms (SANS) were used to assess the positive and negative symptoms in experimental and placebo arms at 12 weeks. The PANSS total scale includes positive and negative subscales. For both subscales, the score ranges from 7-49 and total PANSS score ranges from 30-210. The total scale is a summation of all the subscales. The SANS score ranges from 0-100. For all scales, a greater score represents a worse outcome.
Time frame: 12 weeks
Body composition as estimated by waist to hip ratio in both experimental and placebo arms at 12 weeks.
Time frame: 12 weeks
Body composition estimated by percent total body fat as measured by a dual energy absorptiometry (DXA) scan in both experimental and placebo arms at 12 weeks.
University of Massachusetts, Worcester
Other
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