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临床试验/NCT03670641
NCT03670641已完成4 期

Remission Through Early Monitored Insulin Therapy - Duration Month

Sandra Sobel1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2019年3月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
Change in Baseline A1C and A1C Measured at 3 Month Intervals up to 12 Months

研究概览

简要总结

REMIT-DM is a feasibility pilot study where participants will be recruited soon after their diagnosis of type 2 diabetes to be placed immediately on insulin therapy for maximum of four weeks with titrations of insulin guided by glucose levels and trends provided by a continuous glucose monitor (CGM), with the purpose of achieving diabetes remission.

详细描述

REMIT-DM is a feasibility pilot study that aims to show that previously published diabetes remission through early use and titration of short-term insulin therapy is possible and safe in the ambulatory diverse American population of patients with T2D, with continuous glucose level and trend information provided by CGM. We developed the algorithm based on published diabetes remission studies and include within the algorithm the CGM trend arrows to further refine insulin doses for both safety and efficacy purposes. Data captured by the CGM transmits automatically to the cloud and is accessible at any time of day by the multidisciplinary diabetes team, which includes the certified diabetes educator (CDE) and Endocrinologist. The CGM-guided insulin titration algorithm is designed to achieve euglycemia (defined as fasting CBG < 100 mg/dL, and 2 hour post-prandial CBG < 120 mg/dL) within 2 weeks of initiating insulin therapy, then to help maintain euglycemia for 2 weeks before discontinuing insulin entirely. Ten participants will undergo a maximum of 4 weeks of insulin therapy and will be assessed for remission afterwards to confirm enough recovery of beta cell function. (Complete remission is defined as fasting glycemia <100 mg/dL without use of pharmacological therapy.) Afterwards, we will implement American Diabetes Association (ADA) guidelines for standard glycemic management, as necessary. We will use the data collected during this feasibility study to sharpen the CGM-guided insulin titration algorithm for creation of a T2DM remission mobile application that could then be tested and studied in a larger sample size.

The feasibility study will also take into account clinically meaningful data points e.g. the number of phone calls between the patient and the diabetes team, the patient experience, and patient satisfaction.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • A1C criteria - >7.0
  • Newly diagnosed with T2D within 4 years
  • Lifestyle controlled
  • Subject may be on up to 2 medications for diabetes.
  • Smart phone or home computer compatible with DEXCOM CLARITY software
  • English speaking
  • Assessed by endocrinologist and diabetes educator to be able to perform skills necessary for CGM use and insulin delivery

排除标准

  • Autoimmune Type 1 DM, defined as positive GAD65 or islet cell antibodies
  • Chronic Kidney Disease (CKD) Stage IV or greater
  • Mental and/or cognitive disorder (based on documented disorder and/or assessment of physician or educator)
  • No access to computer for downloading CGM

研究组 & 干预措施

Insulin and CGM Intervention

Experimental

10 individuals with newly diagnosed type 2 diabetes will be started on basal (glargine) bolus (lispro) insulin therapy for up to 4 weeks with titrations guided by continuous glucose monitor (Dexcom G6) to achieve euglycemia and then insulin stopped after 4 weeks with hopes of diabetes remission.

干预措施: Glargine (Drug)

Insulin and CGM Intervention

Experimental

10 individuals with newly diagnosed type 2 diabetes will be started on basal (glargine) bolus (lispro) insulin therapy for up to 4 weeks with titrations guided by continuous glucose monitor (Dexcom G6) to achieve euglycemia and then insulin stopped after 4 weeks with hopes of diabetes remission.

干预措施: Lispro (Drug)

Insulin and CGM Intervention

Experimental

10 individuals with newly diagnosed type 2 diabetes will be started on basal (glargine) bolus (lispro) insulin therapy for up to 4 weeks with titrations guided by continuous glucose monitor (Dexcom G6) to achieve euglycemia and then insulin stopped after 4 weeks with hopes of diabetes remission.

干预措施: Dexcom G6 (Device)

结局指标

主要结局

Change in Baseline A1C and A1C Measured at 3 Month Intervals up to 12 Months

时间窗: Every 3 months up to 1 year

Blood test drawn at baseline and after insulin and CGM-guided titration intervention at 3 month intervals to see if improvement in aggregate A1C value is achieved.

次要结局

  • Number of Patients With Glucose Values <55 mg/dL During 4 Week of Insulin and CGM Intervention(4 weeks)
  • See if Diabetes Distress is Affected With Intervention Via Problem Areas In Diabetes (PAID) - 5 Questionnaire Scale(1 year)
  • Percent Time Glucose Values Remain in Range While Wearing CGM During Insulin Intervention(4 weeks)
  • Number of Participants With A1C of <6.5% After CGM-guided Insulin Therapy Intervention(A1C measures every 3 months up to 1 year)
  • Number of Participants Achieving Euglycemic Glucose Targets Within a 4 Week Period(4 weeks)

研究者

发起方
Sandra Sobel
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Sandra Sobel

Assistant Professor

University of Pittsburgh

研究点 (1)

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