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临床试验/NL-OMON33022
NL-OMON33022已完成不适用

Glucagon challenge in patients with type 2 diabetes mellitus - Glucagon challenge T2DM

Centre for Human Drug Research0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Type 2 diabetes mellitus controlled by oral antidiabetics (except for PPAR-gamma agents) for at least one year;
  • - Age 18 to 65 years;
  • - Males or females (with regular menstrual cycles if premenopausal);
  • - Able and willing to provide written informed consent.

排除标准

  • - Use of insulin or PPAR-gamma agents;
  • - Glycated hemoglobin (HbA1c) > 8%;
  • - BMI <= 22 kg/m2 and >= 35 kg/m2;
  • - Any evidence of cardiovascular, pulmonary, renal, hepatic or other major organ system disease as determined by history, physical examination, and routine laboratory tests;
  • - Uncontrolled hypertension (systolic blood pressure >= 150 mm Hg or a diastolic blood pressure >= 95 mm Hg);
  • - Use of medication known to affect glucose homeostasis (except for biguanides and sulphonylureas), anti-inflammatory drugs, non-selective beta blockers such as propranolol, oral anticoagulants, systemic glucocorticoids or other immunosuppressive drugs;
  • - Use of prescription or over-the-counter drug(s) to promote weight loss;
  • - Pregnancy or breastfeeding;
  • - Not able or willing to use an acceptable contraceptive method for study duration for females (hormonal contraceptives, intra-uterine device or condom/pessary);
  • - Not able and willing to refrain from smoking and/or xanthine use on study day;
  • - Positive test result for HIV, hepatitis B virus, and/or hepatitis C virus;
  • - History of alcohol or drug abuse;
  • - Undergoing or have undergone treatment with an investigational drug, biologic agent or device within 90 days prior to screening
  • - Blood donation within three months and plasma donation within two weeks of screening.

研究者

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