跳至主要内容
临床试验/EUCTR2012-005404-17-DK
EUCTR2012-005404-17-DK进行中(未招募)1 期

Treatment of antipsychotic associated obesity with a GLP-1 Analogue: the TAO study - Treatment of antipsychotic associated obesity

Center for Neuropsychiatric Schizophrenia Research0 个研究点目标入组 45 人开始时间: 2013年1月2日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age: 18 - 65 years
  • Diagnosis in the schizophrenic spectrum (ICD-10: F20.x, F25.x)
  • Treatment with a least one antipsyhcotic agent (FGS/SGA) for a least 3 months
  • BMI = 30 kg/m2
  • HbA1c < 6,5 %
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 80
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Active abuse of psychoactive drugs (ICD-10: F1x.2 (not nicotine))
  • Contradictions to MRI (metalimplant, pacemaker, claustrofobia, =150 kg (max. weight in the MR scanner))
  • Former headtrauma with loss of conciousness more than 5 minutes
  • Severe medical condition/illness
  • Allergi towards exenatide (Bydureon®)
  • Suicidality
  • Forensic psychiatry patient
  • Conditions, who according to Sponsor or Invesigator are not fit for joining the investigation

研究者

发起方
Center for Neuropsychiatric Schizophrenia Research

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