EUCTR2013-001407-36-AT进行中（未招募）不适用
Assessment of Hepatic Glucose Production Following Repeated Glucagon Administration in Type 1 Diabetes Patients
适应症
相关药物
试验速览
- 阶段
- 不适用
- 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
- All
入选标准
- •Type 1 diabetes treated with multiple daily insulin injections or
- •continuous subcutaneous insulin infusion for 12 months
- •Male or female aged 18-65 years (both inclusive)
- •HbA1c < 10%
- •Informed consent obtained after being advised of the nature of the study
- •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 7
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Pregnancy, breast-feeding, intention of becoming pregnant, or not usingadequate contraception
- •Any disease or condition which would interfere with the subject's safety
- •Skin pathology or condition prohibiting needle insertion/glucagon
- •administration as judged by the investigator
- •Severe acute deseases
- •Current participation in another clinical study
- •Uncontrolled hypertension
- •Clinically overt diabetic complications
- •Mental incapacity, unwillingness, or language barriers precluding
- •adequate understanding or cooperation
- •Taking any vasoactive substances or anticoagulatory medication
- •Use of a medication that significantly impacts glucose metabolism
- •i.e. oral ot topical steroids, except in the case of a stable state with a minimum duration of at least 3 months preceeding the study as well asunder the condition that the state remain stable for the duration of the study
- •Symptomatic coronary artery disease
- •Blood donation within 3 months preceeding the study
研究者
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