跳至主要内容
临床试验/NCT07045298
NCT07045298尚未招募不适用

Real-Time Continuous Glucose Monitoring for the Management of Patients With Type 2 Diabetes and Acutely Decompensated Heart Failure

Emory University1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2026年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
140
试验地点
1
主要终点
Mean Daily BG concentration after discharge (DC)

研究概览

简要总结

Heart failure (HF) is a major cause of hospital admissions in the US, with over 6 million hospital days annually.

More than 40% of hospitalized patients with HF have diabetes mellitus (DM), which increases the risk of recurrent hospitalizations for HF with reduced and preserved ejection fraction by more than two-fold. Current methods for assessing glycemic control do not consider fluctuations in blood glucose levels, known as glycemic variability. High glycemic variability is a poor prognostic marker for HF re-hospitalizations. Given the significant prevalence and impact of DM in individuals with HF, it is crucial to examine whether improving glycemic control and avoiding hypoglycemia could lead to a decrease in HF readmissions. Real-time continuous glucose monitoring (rt-CGM), which provides glucose measurements as frequently as every 5 minutes, has improved glycemic control in insulin-treated adults with DM compared to the standard of care, capillary point-of-care blood glucose testing (POC). Researchers will monitor participants during their hospital stay and 3 months after discharge.

详细描述

HF is one of the leading causes of hospitalization among older adults. Nearly 1 in 4 HF patients are readmitted within 30 days of discharge and despite various strategies, the re-hospitalization rates remain high. HF hospitalization has an impact on morbidity, mortality, and healthcare costs. Therefore, it is crucial to identify and implement effective strategies to reduce the health and economic burden of HF re-hospitalization. Diabetes mellitus (DM) is one of the most common comorbidities in HF, impacting approximately a third of all patients. Several studies have reported that HF patients with DM have higher rates of recurrent HF hospitalizations, longer durations of hospital stay, and significantly higher mortality compared to HF patients without DM. Given the high prevalence and impact of DM on HF prognosis, it is important to understand how optimizing DM control can affect and improve the prognosis in this population. Glucose monitoring is central to safe and effective management for individuals with DM, particularly those using insulin. Recent studies have shown that real-time (rt) continuous glucose monitoring (CGM), by providing glucose measurements as often as every 5 minutes, low and high glucose alerts, and glucose trend information, with the potential to better inform diabetes management decisions compared with episodic self-monitoring with a blood glucose meter.

This pilot study will examine the potential benefits of remote glucose monitoring by rt-CGM-driven decisions for the hospital and post-discharge management patients with comorbid HF and DM.

研究设计

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

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults 18 to 90 years admitted with a diagnosis of acute decompensated heart failure (ADHF), New York Heart Association (NYHA) class II, III, or IV symptoms (Aim 1) and discharged with a clinical diagnosis of ADHF (Aim 2).
  • •Patients with diabetes treated with diet alone or oral antidiabetic agents, Glucagon-like peptide-1 receptor agonists (GLP1-RAs), or insulin after discharge

排除标准

  • •Age < 18 or > 90 years;
  • •Patients with a history of type 1 diabetes;
  • •Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study;
  • •Patients on ventricular assist devices;
  • •History of a heart transplant or listed for a heart transplant;
  • •History of cardiac surgery (within 90 days before enrollment) or planned cardiac interventions within the following 6 months;
  • •Female participants who are pregnant or breastfeeding at the time of enrollment into the study;
  • •Hospice care or expected life expectancy of less than 6 months;
  • •Patients who are expected to require Magnetic Resonance Imaging (MRI) procedures during hospitalization or after discharge.

研究组 & 干预措施

POC glucose meter with Blinded CGM (Control/standard of care)

Active Comparator

Participants in the standard-of-care study arm will be provided with a Bluetooth-enabled blood glucose (BG) meter and testing supplies. A blood glucose monitoring account will be established and linked to the research site. Participants will be asked to perform glucose testing from 1- 3x daily. Testing would involve a minimum of once-daily tests that should include random fasting and post-prandial measurements. All participants will also be wearing blinded CGM devices. Providers will adjust oral agents or insulin doses based on POC results.

干预措施: POC BG + Blinded CGM (Diagnostic Test)

Real Time CGM (RT-CGM)

Experimental

Participants in the CGM group will wear a Libre 2 rt-CGM with hypoglycemia and hyperglycemia alarms, and providers will adjust insulin therapy based on CGM profile information. All participants will be instructed on CGM placement and care. Diabetes educators will provide training sessions in the CGM system. The diabetes educator will educate subjects on how the CGM system differs from the traditional blood glucose (BG) meter

干预措施: Libre 2 rt-CGM (Device)

结局指标

主要结局

Mean Daily BG concentration after discharge (DC)

时间窗: After hospital discharge up to 12 weeks

Glucose levels measured by RT-CGM compared to traditional glucose monitoring testing (POCT-BG)

Frequency of clinically significant hypoglycemia after discharge

时间窗: After hospital discharge up to 12 weeks

The mean number of clinically significant hypoglycemia (BG \< 54 mg/dL (\<3.0 mmol/L)) events. Measurements by the POCT glucose monitoring testing (control) and real-time CGM (rt-CGM).

Frequency of overall and nocturnal hypoglycemia events after discharge

时间窗: After hospital discharge up to 12 weeks

The mean number of events of nocturnal hypoglycemia per participant by control (blinded CGM) and real time CGM group. Nocturnal hypoglycemia occurs between 12:00 midnight and 6:00 ante meridiem (AM). Hypoglycemia is defined as BG \< 70 mg/dL (\<3.9 mmol/L) and clinically significant hypoglycemia is defined as BG \< 54 mg/dL (\<3.0 mmol/L).

Percentage of glucose readings and time within target of 70 - 180 mg/dl

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percent of BG readings: 70-180 mg/dL measured by the control (blinded CGM) and rt-CGM.

Percentage of time within target of 70 - 180 mg/dl

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percentage of time with BG: 70-180 mg/dL measured by the control (blinded CGM) and real-time CGM

Frequency of hyperglycemia > 180 mg/dl and >250 mg/dl

时间窗: After hospital discharge up to 12 weeks

Number of events with hyperglycemia, defined as BG between 181 mg/dl and 249 mg/dl by traditional glucose monitoring testing (control) and real-time CGM group.

Percent of time with hyperglycemia

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percentage of the time with hyperglycemia \> 180 mg/dl and \> 250 mg/dl by traditional glucose monitoring testing (control) and by CGM (real-time)

Glycemic variability

时间窗: After hospital discharge up to 12 weeks

Glycemic variability will be calculated by glucose values obtained from the control (blinded CGM) and rt-CGM devices using standard deviation and coefficient of variation. It is designed to assess major glucose swings and exclude minor ones

Mean Daily BG concentration after discharge (DC)

时间窗: After hospital discharge up to 12 weeks

Glucose levels measured by RT-CGM compared to traditional glucose monitoring testing (POCT-BG)

Frequency of clinically significant hypoglycemia after discharge

时间窗: After hospital discharge up to 12 weeks

The mean number of clinically significant hypoglycemia (BG \< 54 mg/dL (\<3.0 mmol/L)) events. Measurements by the POCT glucose monitoring testing (control) and real-time CGM (rt-CGM).

Frequency of overall and nocturnal hypoglycemia events after discharge

时间窗: After hospital discharge up to 12 weeks

The mean number of events of nocturnal hypoglycemia per participant by control (blinded CGM) and real time CGM group. Nocturnal hypoglycemia occurs between 12:00 midnight and 6:00 ante meridiem (AM). Hypoglycemia is defined as BG \< 70 mg/dL (\<3.9 mmol/L) and clinically significant hypoglycemia is defined as BG \< 54 mg/dL (\<3.0 mmol/L).

Percentage of glucose readings and time within target of 70 - 180 mg/dl

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percent of BG readings: 70-180 mg/dL measured by the control (blinded CGM) and rt-CGM.

Percentage of time within target of 70 - 180 mg/dl

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percentage of time with BG: 70-180 mg/dL measured by the control (blinded CGM) and real-time CGM

Frequency of hyperglycemia > 180 mg/dl and >250 mg/dl

时间窗: After hospital discharge up to 12 weeks

Number of events with hyperglycemia, defined as BG between 181 mg/dl and 249 mg/dl by traditional glucose monitoring testing (control) and real-time CGM group.

Percent of time with hyperglycemia

时间窗: After hospital discharge up to 12 weeks

Glycemic control will be measured by the percentage of the time with hyperglycemia \> 180 mg/dl and \> 250 mg/dl by traditional glucose monitoring testing (control) and by CGM (real-time)

Glycemic variability

时间窗: After hospital discharge up to 12 weeks

Glycemic variability will be calculated by glucose values obtained from the control (blinded CGM) and rt-CGM devices using standard deviation and coefficient of variation. It is designed to assess major glucose swings and exclude minor ones

次要结局

  • Composite number of HF re-hospitalization, emergency department/urgent clinic visits for HF management(After hospital discharge up to 12 weeks)
  • Participants with symptoms of HF using the Chronic Heart Failure Questionnaire (CHQ-SAS)(Baseline, 6 and 12 weeks)
  • Quality of life measures using Kansas City Cardiomyopathy Questionnaire (KCCQ)(Baseline, 6 and 12 weeks)
  • Six-minute walk distance (6MWD)(Baseline, 6 and 12 weeks)
  • Composite number of HF re-hospitalization, emergency department/urgent clinic visits for HF management(After hospital discharge up to 12 weeks)
  • Participants with symptoms of HF using the Chronic Heart Failure Questionnaire (CHQ-SAS)(Baseline, 6 and 12 weeks)
  • Quality of life measures using Kansas City Cardiomyopathy Questionnaire (KCCQ)(Baseline, 6 and 12 weeks)
  • Six-minute walk distance (6MWD)(Baseline, 6 and 12 weeks)

研究者

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

Kasra Moazzami

Assistant Professor

Emory University

研究点 (1)

Loading locations...

相似试验