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临床试验/NL-OMON47966
NL-OMON47966已完成不适用

The effect of acute whole-body heat exposure on liver insulin sensitivity and substrate metabolism - Heat and hepatic insulin sensitivity

niversiteit Maastricht0 个研究点目标入组 14 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
14

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • * Signed informed consent
  • * Men and women
  • * Caucasian / white western European
  • * Aged 45-65 years at the start of the study
  • * Body mass index (BMI) 27-35 kg/m2
  • * Stable dietary habits (no weight loss or gain of more than 5 kg in the past 3
  • * Stable sedentary lifestyle (not more than 2 hours of sports per week)
  • * Women after their menopause, meaning cessation of menses for at least 24
  • months) and only if they are not under hormonal treatment
  • * Suitable veins for cannulation or repeated venapuncture
  • * Generally healthy, no medication use that interferes with metabolism, no
  • signs of active cardiovascular disease, liver or kidney malfunction. If
  • volunteers need medication, it will be reviewed with the dependent physician on
  • individual basis.

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • * Type 2 Diabetes
  • * Men Haemoglobin <8.4mmol/L, women haemoglobin <7.8 mmol/L
  • * Signs of active uncontrolled hypertension, liver or kidney malfunction
  • * Cardiac problems and cardiovascular diseases, such as congestive heart
  • failure, angina pectoris, cardiac infarction and arrhythmias
  • * Any medical condition requiring treatment and/or medication that might
  • interfere with the investigated parameters. All medical conditions/medications
  • will be reviewed with the dependent physician and in-/exclusion will be decided
  • on individual basis
  • * Unstable body weight (weight gain or loss >3kg in the past three months)
  • * Participation in another biomedical study within 1 month prior to screening
  • * Participants, who do not want to be informed about unexpected medical
  • findings, or do not wish that their treating physician will be informed, cannot
  • participate in this study
  • * Blood donation three month prior to study and three month after finishing
  • * Alcohol consumption of >2 servings per day for men and >1 serving per day for
  • * Smoking in the past 6 months
  • A medical doctor will judge participation eligibility based on the medical
  • history questionnaire, medication use and fasting blood parameters. If the
  • medical doctor advises that someone cannot participate, they will be excluded
  • from enrolment.

研究者

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