EUCTR2014-002341-22-AT进行中(未招募)不适用
Evaluation of the Effect of Glucagon Solutions on the Glucose Concentration at the Subcutaneous Administration Site in Type 1 Diabetic Patients.
Medizinische Universität Graz; Universitätsklinik für InnereMedizin; Abteilung für Endokrinologie und Stoffwechsel0 个研究点开始时间: 2014年6月11日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •- 18 to 64 years of age, both inclusive
- •- Type 1 diabetes treated with CSII or MDI
- •- HbA1C < 10%
- •- BMI between 20 and 30 kg/m2
- •- Signed informed consent before any study-related activities
- •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 10
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •- Severe acute diseases
- •- Clinically overt diabetic complications
- •- Mental incapacity, unwillingness or language barriers precluding adequate understanding or co-operation
- •- Taking of any vasoactive substances or anticoagulation medication
- •- Diseases of the skin which could interfere with application of catheters as judged by the investigator
- •- Uncontrolled hypertension
- •- Use of a medication that significantly impacts glucose metabolism (e.g. oral or topical steroids) except in the case of a stable state with a minimum duration of at least three months preceding the study as well as under the condition that the state remain stable for the duration of the study
- •- No superficial veins for catheter insertion as judged by the investigator
- •- Pregnancy, breastfeeding, intention of becoming pregnant or not using adequate contraception.
- •- Any disease or condition which the investigator or treating physician feels would interfere with the trial or the safety of the subject
- •- Concurrent participation in another study
研究者
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