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临床试验/NCT04997512
NCT04997512尚未招募不适用

FreeSTyle LibRe and hospitAl Admissions, morTality and qUality of Life in High Risk Type 2 diabeteS Patients

University of Leeds2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
300
试验地点
2
主要终点
Mortality at 2 years

研究概览

简要总结

This study aims to investigate the utility of a combination of structured nurse led intervention and the use of Freestyle libre in adults with type 2 diabetes who have suffered an episode of severe hypoglycaemia in terms of mortality, unscheduled healthcare contacts and quality of life.

详细描述

It is increasingly recognised that hypoglycaemia carries risk to individuals with all forms of diabetes. Research has shown high rate of mortality in those with type 2 diabetes following an episode of severe hypoglycaemia and a previous pilot trial conducted in the UK suggested that this could be improved by a structured nurse led intervention aimed at modifying glycemic therapy to avoid hypoglycaemia, instigating regular blood glucose monitoring and providing education to participants on common triggers for hypoglycaemia and how to avoid them.

In this trial, the investigators will randomise individuals with type 2 diabetes who have suffered an episode of severe hypoglycaemia requiring emergency service call out to two arms. One arm will receive standard of care/treatment as usual and the other will receive a structured nurse led intervention as well as the use of a flash glucose monitoring system, Freestyle libre.

Active participation in the trial for both arms will be a total of twelve months (with the main intervention months 0-6.) Participants electronic records will be analysed for death and unscheduled healthcare contacts for a total of two years after recruitment.

The primary outcome measure is mortality between groups. Secondary outcomes include the use of estimated HbA1c (a variable produced by the freestyle libre device) compared to laboratory HbA1c, quality of life measures, effects on glycemic control and the number of unscheduled healthcare contacts.

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

盲法说明

Unable to mask participants and trailists due to study design.

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Mortality at 2 years

时间窗: 2 years

Rates of death between groups at 2 years

次要结局

  • All-cause mortality at 1 year(12 months)
  • Cardiovascular mortality at 2 years(2 years)
  • Cardiovascular mortality at 1 year(1 year)
  • Change from baseline in HbA1c(6 months)
  • Scores from treatment satisfaction scale (DTSQc)(Tested at 0 and 6 months)
  • Number of unscheduled healthcare contacts(2 years after randomisation)
  • Comparison between estimated HbA1c and laboratory HbA1c(6 months)
  • Scores from Diabetes distress scale(Tested at 0 and 6 months)
  • Scores from GOLD score(Tested at 0 and 6 months)
  • Scores from diabetes quality of life scale (DQOL)(Tested at 0 and 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ramzi Ajjan

Professor of metabolic medicine

University of Leeds

研究点 (2)

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