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临床试验/NCT02167620
NCT02167620已完成4 期

Metformin in Co-morbid Diabetes or Prediabetes and Serious Mental Illness

Centre for Addiction and Mental Health1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2014年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
35
试验地点
1
主要终点
Improvement in HbA1C derived from Oral glucose tolerance test (Matsuda, index of insulin sensitivity; area under glucose curve; insulin secretion sensitivity index-2 (ISSI-2))

研究概览

简要总结

Schizophrenia is associated with a lifespan shortened by 20 years, due to cardiovascular disease (CVD), with antipsychotic (AP) medications understood to contribute to this risk through associated metabolic side-effects. Metformin, a medication used to treat prediabetes, and diabetes in the general population, holds promise with regard to reduction of AP-related metabolic problems, but has not been directly tested in early episode patients beyond weight loss, nor specifically in patients with diabetes or prediabetes and psychosis. We propose to replicate findings that metformin can reduce weight gain, and dysglycemia uniquely focusing on an early episode population diagnosed with prediabetes or diabetes. To help determine long-term risk/benefit of adjunctive metformin, we propose to look at changes in abdominal and liver fat, two well-established risk factors for CVD. Given links between dysglycemia, obesity with hippocampal volume loss and cognitive dysfunction, we will explore if improvements in metabolic indices are associated in changes in cognition and brain structure.

详细描述

This is a 16 week, double-blind, randomized pilot study, which proposes to recruit 24 patients with schizophrenia, or schizoaffective disorders (DSM 5), who are overweight or obese (BMI >25) and have prediabetes or type 2 diabetes. Randomization occurs on a 2:1 basis, with 16 patients randomised to metformin, and 8 to placebo. Metfomin/placebo is dispensed monthly. The baseline and /or screening visit includes a physical exam (including anthropometric measures), medical history, fasting blood work (glucose, insulin, HbA1c, lipids, electrolytes, thyroid, liver/kidney function), in addition to a urine drug screen. Women of child-bearing age are given a pregnancy test. Patients who meet inclusion criteria and consent to the study have an oral glucose tolerance test (OGTT), and a baseline abdominal and brain MRI (to respectively assess visceral adiposity, a key risk factor for CV disease, and hippocampal volumes). Anthropometric measures and pill counts are repeated bi-weekly. At week 8, fasting insulin/glucose, HbA1C, and liver function tests are measured. End of study measures (week 16), include the same panel of bloodwork conducted at baseline, as well as a repeat OGTT, and an abdominal and brain MRI. Rountine psychopathology scales, including BPRS, CGI, and CDS will be measured at baseline, and week 16. The Brief Assessment of Cognition in Schizophrenia (BACS) will also be completed at baseline, and study end.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
17 Years 至 45 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients within 5 years of diagnosis of schizophrenia, schizoaffective disorder , or bipolar disorder(DSM V), or those younger than 40 years old, regardless of duration of illness
  • Co-morbid diagnosis of prediabetes or diabetes (Canadian or American Diabetes Association criteria)

排除标准

  • Patients with co-morbid axis, other than nicotine dependence, or cannabis abuse
  • Patients with liver, or renal dysfunction,
  • Patients with a positive drug urine screen (other than cannabis or nicotine)
  • Females with a positive pregnancy test will be excluded.
  • Prior trial with metformin, and reported lack of tolerability
  • Patients with an A1C > 9.5%, or symptomatic hyperglycemia with metabolic decompensation

研究组 & 干预措施

Metformin

Placebo Comparator

Metformin/ placebo will be dispensed on a biweekly basis, and pill counts conducted at each visit.

干预措施: Metformin (Drug)

Placebo

Placebo Comparator

Metformin/ placebo will be dispensed on a biweekly basis, and pill counts conducted at each visit.

干预措施: Placebo (Drug)

结局指标

主要结局

Improvement in HbA1C derived from Oral glucose tolerance test (Matsuda, index of insulin sensitivity; area under glucose curve; insulin secretion sensitivity index-2 (ISSI-2))

时间窗: 3 years

HbA1c value assessment

次要结局

  • Improvements in cognition(3 years)
  • Decreases in hepatic adiposity(3 years)
  • Greater than 5% decrease in body weight(3 years)
  • Decreases in visceral adiposity(3 years)
  • Improvements in hippocampal volume(3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Margaret Hahn

Clinician/Scientist

Centre for Addiction and Mental Health

研究点 (1)

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