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临床试验/EUCTR2016-000810-31-NL
EUCTR2016-000810-31-NL进行中(未招募)1 期

Impact of L-Carnitine infusion on Lipid induced Insulin resistance - Carnitine infusion and Insulin resistance

Maastricht University0 个研究点开始时间: 2016年3月14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)

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
Male

入选标准

  • Healthy (as determined by responsible physician based on a medical questionnaire)
  • Age: 18-40 years
  • Normal BMI: 18-25 kg/m2
  • Stable dietary habits
  • No use of medication interfering with investigated study parameters (as determined by responsible physician)
  • 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 18
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Haemoglobin levels < 7.8 mmol/L
  • Uncontrolled hypertension
  • Use of anticoagulants
  • Engagement in exercise > 3 hours a week
  • Being vegetarian or vegan (because of altered whole body carnitine status)
  • Alcohol and/or drug abuse
  • Unstable body weight (weight gain or loss > 5kg in the last 3 months)
  • Significant food allergies/intolerances (seriously hampering study meals)
  • Participation in another biomedical study within 1 month before the first study visit, which would possibly hamper our study results
  • Medication use known to hamper subject’s safety during the study procedures
  • Medication use known to interfere with investigated study parameters
  • Subjects with contra-indications for MRI
  • Subjects who intend to donate blood during the intervention or subjects who have donated blood less than three months before the start of the study
  • Subjects who do not want to be informed about unexpected medical findings
  • Subjects who do not want that their treating physician is informed

研究者

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