跳至主要内容
临床试验/DRKS00021284
DRKS00021284
已完成
1 期

A placebo-controlled, randomized, double-blind trial to investigate the impact of dapagliflozin on the development of diabetic ketoacidosis and intermediate metabolism in type 1 diabetes using a dual stable tracer method: A safety study investigating the fuel shift theory in the human model - AZ02_Dapa_T1D

Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Abteilung für Endokrinologie und Diabetologie0 个研究点目标入组 17 人2020年4月8日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
E10
发起方
Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Abteilung für Endokrinologie und Diabetologie
入组人数
17
状态
已完成
最后更新
去年

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2020年4月8日
结束日期
2020年9月28日
最后更新
去年
研究类型
Interventional
性别
Male

研究者

发起方
Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Abteilung für Endokrinologie und Diabetologie

入排标准

入选标准

  • Men aged 18\-55 years (both inclusive) at the time of signing the consent form
  • Diagnosis of type 1 diabetes mellitus.
  • C\-peptide (fasting value) \= 0\.07 ng/ml (\= 0\.02 nmol/L).
  • Stable insulin therapy for at least 6 months prior to screening by continuous subcutaneous insulin infusion (CSII).
  • Body Mass Index (BMI) between 20\.0 and 35\.0 kg/m2 (both inclusive)
  • HbA1c \= 85,8 mmol/mol (\= 10,0 %).

排除标准

  • People with muscular symptoms of hyperglycemia (tingling, pain). Known or suspected hypersensitivity to experimental products or other related products. History of severe allergy to medicines or foods or a history of severe anaphylactic reactions.
  • Presence of clinically relevant respiratory, cardiovascular, endocrine (except those related to diabetes mellitus), severe liver dysfunction, or other conditions that the investigator deems could compromise safety or compliance with the protocol. Receipt of an investigational medicinal product (IMP) within one month (or 5 half\-life periods, whichever is longer) prior to screening. Uncontrolled hypertension is defined as blood pressure at screening (after 5 min rest) outside the range 90\-160 mmHg for systolic or 50\-100 mmHg for diastolic. Acute symptomatic (according to the investigator's assessment) urinary tract or genital infection, chronic or recurrent (\= 3\-year episodes) cystitis. Proliferative retinopathy or maculopathy (requiring treatment) and/or severe neuropathy, especially autonomic neuropathy, as determined by the investigator. Use of medications that may interfere with the interpretation of study results or are known to cause clinically relevant disturbances in insulin action, glucose utilization, or recovery from hypoglycemia (in the investigator's judgment). Hemoglobin \< 12\.5 g/dl, serum creatinine level \= 1\.43 mg/dl (\= 126 µmol/L) (male), alanine transaminase (ALT) or alkaline phosphatase (ALP) \> 2\.5 x ULN. Estimated glomerular filtration rate (eGFR) \< 60 mL/min/1\.73 m². Positive laboratory result for screening test for HIV, hepatitis B and/or hepatitis C. Surgery or trauma with significant blood loss (more than 500 mL) within the last 3 months before screening. Smoker (defined as a subject who smokes at least five cigarettes or the equivalent product per day) who is unable or unwilling to refrain from smoking or from using nicotine gum or transdermal nicotine patches during the inpatient period Known or suspected alcohol or drug/chemical abuse (as determined by the investigator) or positive result of an alcohol test or positive result of a drug abuse test.

结局指标

主要结局

未指定

相似试验

尚未招募
4 期
A placebo-controlled, randomized, double-blind trial of the effects of modified release 4-aminopyridine on upper limb impairment in Multiple SclerosisMultiple SclerosisNeurological - Multiple sclerosis
ACTRN12613000331730Austin Health60
进行中(未招募)
1 期
A study to investigate the efficacy and tolerability of the drug ESO-101 in adult patients with inflammation of the esophagusActive eosinophilic esophagitisMedDRA version: 20.1Level: PTClassification code 10064212Term: Eosinophilic oesophagitisSystem Organ Class: 10017947 - Gastrointestinal disordersTherapeutic area: Diseases [C] - Digestive System Diseases [C06]
EUCTR2020-000082-16-PLEsoCap AG42
进行中(未招募)
4 期
Can treatment with Cerebrolysin improve recovery after acute ischemic stroke?Radiologically confirmed acute ischemic stroke with onset within 72 hours prior to screeningCirculatory SystemAcute ischemic stroke
ISRCTN88122184The foundation for the study of neuroscience and neuroregeneration290
进行中(未招募)
1 期
A study to investigate the efficacy and tolerability of the drug ESO-101 in adult patients with inflammation of the esophagusActive eosinophilic esophagitisMedDRA version: 20.1Level: PTClassification code 10064212Term: Eosinophilic oesophagitisSystem Organ Class: 10017947 - Gastrointestinal disordersTherapeutic area: Diseases [C] - Digestive System Diseases [C06]
EUCTR2020-000082-16-NLEsoCap AG42
招募中
2 期
A randomized, placebo-controlled, double-blind trial evaluating the efficacy, tolerability and safety of ESO-101 in adult patients with active eosinophilic esophagitischronic inflammation of the esophaguseosinophilic esophagitis10017969
NL-OMON52665EsoCap AG10