跳至主要内容
临床试验/NCT04428762
NCT04428762撤回不适用

Glycemic Control and Quality of Life With i- Port Advance in Pediatric T1DM: Multi Center Crossover and Prospective Assessment

Assaf-Harofeh Medical Center0 个研究点开始时间: 2020年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Life quality and satisfaction measures

研究概览

简要总结

The incidence of T1DM in children, especially infants under 4 years of age, is increasing in the last decade. Not all patients are willing or able, from different reasons, to be treated with insulin pumps. This portion of patients' needs subcutaneous insulin injections, at lest 4 injections per day, sometimes up to 8 injections per day.

The recommended treatment is insulin injection before each carbohydrate content meal. Since each injection may lead to pain, many patients do not inject all recommended doses. The solution could be: eat with no bolus, or not to correct glucose level to retrain from pain sensation. I-Port use is able to address this issue by reducing the pain sensation accompanied with the injection. I-Port advance may give a technological solution to non-insulin pump T1DM pediatric patients.

There are no reports in the literature of the use of iport in children and youth. This information is essential since 95% of pediatric diabetes mellitus cases are insulin dependent and require multiple injections. Better balanced diabetes in childhood may prevent complications to long range and long-term diabetes therapy. Moreover, if discovered safe, the iport can be used also for other subcutaneously delivered medication in children, such as somtostatin analog, human growth hormone and clexane Study is designed as 2 parts. Initial part is a cross over design to compare between ipor use an injections regarding glucose in range, side effects and quality of life.

Second part is designed as prospective. To assess glycemic control with iport use or 3 months .

详细描述

study withdrawn Nor relevant

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
1 Year 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with type 1 diabetes mellitus
  • Insulin injection ≥2 per day for at least a week.
  • Use of MDI insulin: Novorapid, Humalog or Apidra.
  • Ability and willingness to perform at least 3 daily self-measured plasma glucose profiles
  • Ability and willingness to adhere to the protocol. -

排除标准

  • Insulin pump use
  • Mix insulin use -

结局指标

主要结局

Life quality and satisfaction measures

时间窗: 3 months from patient first enrollment

Life quality measure before and after I-Port Advance use by questionnaire-delta of score

Adverse effect

时间窗: 3 months from patient first enrollment

Number of Adverse effect while using I-port-clinical

次要结局

  • Glycemic control evaluation(3 months from patient first enrollment)

研究者

申办方类型
Other Gov
责任方
Sponsor

相似试验