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临床试验/NCT02359617
NCT02359617
已完成
不适用

Continuous Glucose Sensing at the Site of Subcutaneous Insulin Administration: Evaluation of a Novel Single-Port Treatment Approach in Type 1 Diabetic Patients During a 1-Day Stay in a Clinical Research Center and a 6-Day Period at Home

Medical University of Graz1 个研究点 分布在 1 个国家目标入组 10 人2013年2月

概览

阶段
不适用
干预措施
insulin delivery
疾病 / 适应症
Type 1 Diabetes
发起方
Medical University of Graz
入组人数
10
试验地点
1
主要终点
Mean absolute relative difference between sensor readings and capillary glucose readings
状态
已完成
最后更新
11年前

概览

简要总结

The study seeks to evaluate a novel treatment approach for performing continuous real-time glucose sensing and insulin delivery at the same subcutaneous tissue site.

详细描述

The treatment of type 1 diabetes usually comprises the measurement of glucose in blood obtained by finger pricking and the administration of insulin via subcutaneous bolus injection or continuous subcutaneous infusion. This study seeks to test a new treatment approach where glucose sensing and insulin administration are combined and performed at a single subcutaneous tissue site (single-port treatment approach). A single-port device consisting of a continuous glucose sensor and an insulin infusion cannula is inserted into the subcutaneous tissue of 10 type-1 diabetes patients and used for insulin infusion and simultaneous glucose sensing over a 7-day period. The performance of the single-port device is assessed by comparing the obtained glucose readings with those of a blood glucose meter and an additionally worn control sensor.

注册库
clinicaltrials.gov
开始日期
2013年2月
结束日期
2015年3月
最后更新
11年前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

发起方
Medical University of Graz
责任方
Principal Investigator
主要研究者

Pieber Thomas, MD

MD, Prof. of Medicine

Medical University of Graz

入排标准

入选标准

  • 18 to 65 years of age, both inclusive
  • Type 1 diabetes treated with Continuous Subcutaneous Insulin Infusion (CSII)
  • HbA1C \< 10%
  • Signed informed consent before any study-related activities

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 the catheters and Sensors as judged by the investigator
  • Pregnancy, breastfeeding, intention of becoming pregnant or not using adequate contraception.
  • Increased tendency towards development of hypoglycaemia
  • 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

研究组 & 干预措施

glucose sensing and insulin delivery

Subcutaneous insulin delivery with an insulin pump plus glucose sensing with a continuous glucose sensor placed at the site of subcutaneous insulin delivery. In parallel, capillary glucose determinations using a conventional glucose meter as well as glucose sensing in subcutaneous, insulin-unexposed tissue using a continuous glucose sensor.

干预措施: insulin delivery

glucose sensing and insulin delivery

Subcutaneous insulin delivery with an insulin pump plus glucose sensing with a continuous glucose sensor placed at the site of subcutaneous insulin delivery. In parallel, capillary glucose determinations using a conventional glucose meter as well as glucose sensing in subcutaneous, insulin-unexposed tissue using a continuous glucose sensor.

干预措施: glucose sensing

结局指标

主要结局

Mean absolute relative difference between sensor readings and capillary glucose readings

时间窗: 7 days

Mean absolute relative differences calculated by determining the mean of the absolute value of the percentage difference between paired sensor and capillary glucose concentration

研究点 (1)

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