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Reproducibility of Continuous Glucose Monitoring (CGM) in the Assessment of Glucose Metabolism Disorders in Children With Cystic Fibrosis (CGMUCODIAB)

2026年9月25日 更新者:Hospices Civils de Lyon

Glucose metabolism disorders in cystic fibrosis (CF-GMD) are common and have a negative clinical impact. Screening currently relies on the oral glucose tolerance test (OGTT); however, this procedure is burdensome and complex for both patients and healthcare providers. Continuous glucose monitoring (CGM) is increasingly used in CF centers for CF-GMD screening, either alone or alongside the OGTT. While long-term (one-year) OGTT reproducibility is known to be poor, the short- and medium-term reproducibility of CGM remains unknown. This examination is poised to become a major tool in CF-GMD investigation, upon which critical therapeutic decisions could be based. The primary objective of this project is to evaluate the short-term variability of CGM data.

研究概览

研究类型

介入性

注册 (估计的)

30

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • Bron、法国、69677
        • Hôpital Femme Mère Enfant (HFME)
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

10年 至 17年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Patients aged 10 to 17 years
  • Diagnosed with cystic fibrosis (CF)
  • Managed by the pediatric CF care center (CRCM) of the Groupement Hospitalier Est
  • Patients presenting with one of the following three stages are included: normal glucose tolerance with or without indeterminate glucose tolerance (INDET), impaired fasting glucose (IFG), and impaired glucose tolerance (IGT)

Exclusion Criteria:

  • Patients with treated or untreated diabetes
  • Patients presenting with a pulmonary exacerbation and currently receiving antibiotic therapy
  • Patients participating in another clinical trial that could interfere, in the investigator's judgment, with the study findings
  • Refusal of the patient and/or the legal guardian(s) to participate in the study
  • Pregnant, parturient, or breastfeeding women
  • Persons deprived of liberty by a judicial or administrative decision
  • Persons undergoing psychiatric care
  • Persons admitted to a healthcare or social institution for purposes other than research
  • Persons not affiliated with a social security scheme or beneficiaries of a similar scheme

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:诊断
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Non-diabetic patient with cystic fibrosis

Children aged 10 to 17 years diagnosed with cystic fibrosis (CF). Patients presenting with one of the following three stages are included: normal glucose tolerance with or without indeterminate glucose tolerance (INDET), impaired fasting glucose (IFG), and impaired glucose tolerance (IGT).

Patients will be equipped with a continuous glucose monitoring (CGM) sensor (Dexcom ONE+).

Upon enrollment, patients will be equipped with a continuous glucose monitoring (CGM) sensor (Dexcom ONE+). Sensors will be placed on the posterior aspect of the dominant arm at M0, M3, and M6, and additionally on the non-dominant arm at M0 only, in order to evaluate site-dependent variability. At each time point, the sensors will be worn for 7 days to record various CGM parameters, including glycemic variability (analyzed between M0-M3 and M0-M6).

A 7-day dietary diary will be completed at M0, M3, and M6.

Participants will wear an actigraphy watch during 7 days at M0, M3 and M6

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
The variability of the "time in range" (%) parameter (70-140 mg/dL) between M0 and M3.
大体时间:From enrollment to 3 months

The variability of the "time in range" (%) parameter (70-140 mg/dL) between M0 and M3.

From enrollment to 3 months

次要结果测量

结果测量
措施说明
大体时间
The variability of other CGM parameters between M0 and M3: percentage of time in hypoglycemia (<70 mg/dL)
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: percentage of time in hypoglycemia (<70 mg/dL)

From enrollment to 3 months
The variability of other CGM parameters between M0 and M3: percentage of time in hyperglycemia (>140 mg/dL)
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: percentage of time in hyperglycemia (>140 mg/dL)

From enrollment to 3 months
The variability of other CGM parameters between M0 and M3: glycemic variability (%)
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: glycemic variability (%)

From enrollment to 3 months
The variability of other CGM parameters between M0 and M3: mean glucose level (mg/dL)
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: mean glucose level (mg/dL)

From enrollment to 3 months
The variability of other CGM parameters between M0 and M3: number of glucose excursions >200 mg/dL
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: number of glucose excursions >200 mg/dL

From enrollment to 3 months
The variability of other CGM parameters between M0 and M3: estimated HbA1c (eA1c)
大体时间:From enrollment to 3 months

The variability of other CGM parameters between M0 and M3: estimated HbA1c (eA1c)

From enrollment to 3 months
The variability of CGM parameters between M0 and M6: "time in range" (%) (70-140 mg/dL)
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: "time in range" (%) (70-140 mg/dL)

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: percentage of time in hypoglycemia (<70 mg/dL),
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: percentage of time in hypoglycemia (<70 mg/dL),

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: percentage of time in hyperglycemia (>140 mg/dL),
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: percentage of time in hyperglycemia (>140 mg/dL),

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: glycemic variability (%),
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: glycemic variability (%),

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: mean glucose level (mg/dL),
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: mean glucose level (mg/dL),

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: number of glucose excursions >200 mg/dL
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: number of glucose excursions >200 mg/dL

From enrollment to 6 months
The variability of CGM parameters between M0 and M6: estimated HbA1c (eA1c)
大体时间:From enrollment to 6 months

The variability of CGM parameters between M0 and M6: estimated HbA1c (eA1c)

From enrollment to 6 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): "time in range" (%) (70-140 mg/dL)
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): "time in range" (%) (70-140 mg/dL)

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): percentage of time in hypoglycemia (<70 mg/dL),
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): percentage of time in hypoglycemia (<70 mg/dL),

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): percentage of time in hyperglycemia (>180 mg/dL)
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): percentage of time in hyperglycemia (>180 mg/dL)

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): glycemic variability (%)
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): glycemic variability (%)

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): mean glucose level (mg/dL)
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): mean glucose level (mg/dL)

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): number of glucose excursions >200 mg/dL
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): number of glucose excursions >200 mg/dL

From enrollment to 3 months
The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): estimated HbA1c (eA1c)
大体时间:From enrollment to 3 months

The variability of CGM parameters according to the sensor placement site between M0 and M3 (inter-arm variability): estimated HbA1c (eA1c)

From enrollment to 3 months
The variability of CGM parameters according to physical activity (percentage of daytime activity) : Variation in the number of steps
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to physical activity (percentage of daytime activity), Variation in the number of steps

From enrollment to 3 months and 6 months
The variability of CGM parameters according to body composition (body fat percentage)
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to body composition (body fat percentage) : body fat in kg

From enrollment to 3 months and 6 months
The variability of CGM parameters according to body composition
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to body composition (lean mass percentage) : body fat in kg

From enrollment to 3 months and 6 months
The variability of CGM parameters according to body composition (fat mass percentage in the dominant arm)
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to body composition (fat mass percentage in the dominant arm) : body fat in kg

From enrollment to 3 months and 6 months
The variability of CGM parameters according to body composition (fat mass percentage in the non-dominant arm) : body fat in kg
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to body composition (fat mass percentage in the non-dominant arm) : body fat in kg

From enrollment to 3 months and 6 months
The variability of CGM parameters according to nutritional intake : Daily nutritional intake (kcal)
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to nutritional intake : Daily nutritional intake (kcal)

From enrollment to 3 months and 6 months
The variability of CGM parameters according to nutritional intake : carbohydrates (kg)
大体时间:From enrollment to 3 months ans 6 months

The variability of CGM parameters according to nutritional intake : carbohydrates (kg)

From enrollment to 3 months ans 6 months
The variability of CGM parameters according to nutritional intake : fats (kg)
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to nutritional intake : fats (kg)

From enrollment to 3 months and 6 months
The variability of CGM parameters according to nutritional intake : proteins (kg)
大体时间:From enrollment to 3 months and 6 months

The variability of CGM parameters according to nutritional intake : proteins (kg)

From enrollment to 3 months and 6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2028年2月1日

研究完成 (估计的)

2028年5月1日

研究注册日期

首次提交

2026年9月21日

首先提交符合 QC 标准的

2026年9月25日

首次发布 (实际的)

2026年10月1日

研究记录更新

最后更新发布 (实际的)

2026年10月1日

上次提交的符合 QC 标准的更新

2026年9月25日

最后验证

2026年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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