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临床试验/NCT06414824
NCT06414824终止不适用

The Impact of the isCGM Use on the Hypoglycemic Episodes and Fear of Hypoglycemia in Patients With Newly Diagnosed Type 1 Diabetes

Jagiellonian University4 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2022年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
28
试验地点
4
主要终点
TBR <70 mg/dL

研究概览

简要总结

The aim of this trial is to investigate the impact of FreeStyle Libre use compared to SMBG on hypoglycemia episodes and fear of hypoglycemia in adults aged 18-35 with newly diagnosed type 1 diabetes.

This trial is conducted in university centers in Poland (Bialystok, Krakow, Poznan, Zabrze).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Newly diagnosed type 1 diabetes (diagnosed based on the WHO criteria) no later than 6 months after the diagnosis.
  • Insulin therapy: multiple daily injections,
  • In the investigator's opinion, the participant must be technically capable of using the FreeStyle Libre system

排除标准

  • Current or past use of any continuous glucose monitoring system.
  • Pump therapy.
  • Known allergy to medical adhesives.
  • Oral steroid therapy.
  • Pregnancy or planning pregnancy within the study duration.
  • Breast feeding.
  • Dialysis treatment.
  • Having a pacemaker.
  • Unstable coronary heart disease.
  • Cystic fibrosis.
  • Psychiatric disorders.
  • Severe end-organ damage (kidney, liver, etc) or any uncontrolled disorder.
  • Hospitalization for any reason other than the newly diagnosed type 1 diabetes 6 months prior to inclusion.
  • Participating in another clinical trial that could affect glucose measurements or glucose management.
  • In the investigator's opinion, if the participant is considered unsuitable for inclusion in the study for any other reason.

结局指标

主要结局

TBR <70 mg/dL

时间窗: Baseline and days 14 to 28

Difference in time \<70 mg/dL between intervention and control group assessed in days 14 to 28

Hypoglycemia Fear Survey II

时间窗: Baseline and day 28

Change in HFS II score from baseline to day 28

次要结局

  • HFS II - Worry subscale(Baseline and day 28)
  • TIR(Baseline and days 14 to 28)
  • TAR >250 mg/dl(Baseline and days 14 to 28)
  • HFS II - Behaviour subscale(Baseline and day 28)
  • TAR >180 mg/dl(Baseline and days 14 to 28)
  • DKA(Baseline to day 28)
  • TBR <54 mg/dL(Baseline and days 14 to 28)
  • Severe hypoglycemia(Baseline to day 28)
  • DDS(Baseline and day 28)
  • DTSQ(Baseline and day 28)

研究者

发起方
Jagiellonian University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jerzy Hohendorff

MD, PhD

Jagiellonian University

研究点 (4)

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