The VRIF Trial: Hypoglycemia Reduction With Automated-Insulin Delivery System
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Percentage of Time of Blood Glucose in Range 70-180 mg/dL
研究概览
简要总结
The objective of this pilot study is (i) to test the use of an Artificial Pancreas (AP) System as a viable therapy treatment for two vulnerable populations: 6 to 10 year-old and adults older ≥65 years old with T1D; (ii) to assess cognitive function in children and older adult patients with T1D and examine whether improved glycemic control defined by stable (more than 70% of the day in glycemic range 70-180 mg/dL) control positively influences cognitive function; and (iii) obtain preliminary data to apply to funds to continue with larger and longer clinical trials.
详细描述
This study will evaluate up to 15 subjects in each age group for a period of 8-10 weeks performing neurocognitive tests before and after each intervention. The first study phase will be up to 2 weeks of a training period to allow participants to get acquainted with the use of the CGM if they are not familiar with the use of the device. This training period will be followed by a 4-week sensor-augmented pump (SAP) period using a study CGM and the subject's personal insulin pump. The subjects will return to clinic at the completion of the SAP period and will be trained on the Tandem t:slim X2 with Control-IQ and G6 CGM. At the completion of the system training session, subjects will begin 4-weeks of Closed-Loop Control (CLC). Questionnaires will be completed by the study subject at screening, after completion of SAP and after completion of CLC. Ecological Momentary Assessments (EMAs) and actigraphy data will be collected in the last 14 days of the SAP and CLC periods.
A parent/guardian of the enrolled children will also be asked to participate in all trainings, complete parental Patient-Report Outcomes (PRO) Questionnaires, and collect sleep patterns while wearing the actigraph watch.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 6 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis, based on investigator assessment, of type 1 diabetes for at least one year, using insulin for at least 1 year and using an insulin pump for at least 6 months.
- •Familiarity and use of a carbohydrate ratio for meal boluses by participants and families participating.
- •Age 6-10 years old or 65 years or older
- •Hemoglobin A1c <10%
- •For females of child-bearing potential, not currently known to be pregnant:
- •A negative serum or urine pregnancy test will be required for all females of child-bearing potential. Participants who become pregnant will be discontinued from the study. Also, participants who during the study develop and express the intention to become pregnant within the timespan of the study will be discontinued.
- •For participants <18 years old, living with one or more parent/legal guardian knowledgeable about emergency procedures for severe hypoglycemia and able to contact the participant in case of an emergency.
- •Willing to disable any automated insulin delivery functionality on a personal insulin pump during study, such as Medtronic 670G in auto mode. Predictive low blood glucose suspend, such as Tandem insulin pump with Basal-IQ, will be allowed.
- •Investigator has confidence that the participant and family can successfully operate all study devices and is capable of adhering to the protocol.
- •Willingness to switch to lispro (Humalog) or aspart (Novolog) and to use no other insulin besides lispro (Humalog) or aspart (Novolog) during the study.
- •Total daily insulin dose (TDD) at least 10 U/day.
- •Willingness not to start any new non-insulin glucose-lowering agent during the course of the trial
排除标准
- •Severe hypoglycemia resulting in seizure or loss of consciousness in the 12 months prior to enrollment.
- •Diagnosis of Diabetic Ketoacidosis in the 12 months prior to enrollment.
- •Uncontrolled cardiac disease (e.g. recent myocardial infarction, severe congestive heart failure).
- •Cerebrovascular accident in the 12 months prior to enrollment.
- •Uncontrolled resting arterial hypertension (>160/90 mm Hg).
- •Conditions that would make use of a CGM difficult (e.g., blindness, severe arthritis, immobility).
- •Current use of oral/inhaled glucocorticoids or other medications, which in the judgment of the investigator would be a contraindication to participation in the study.
- •Concurrent use of any non-insulin glucose-lowering agent other than metformin (including GLP-1 agonists, pramlintide, DPP-4 inhibitors, SGLT-2 inhibitors, sulfonylureas).
- •Hemophilia or any other bleeding disorder
- •A condition, which in the opinion of the investigator or designee, would put the participant or study at risk
- •Participation in another pharmaceutical or device trial at the time of enrollment or during the study
- •Employed by, or having immediate family members employed by Tandem Diabetes Care, Inc., or having a direct supervisor at place of employment who is also directly involved in conducting the clinical trial (as a study investigator, coordinator, etc.); or having a first-degree relative who is directly involved in conducting the clinical trial.
结局指标
主要结局
Percentage of Time of Blood Glucose in Range 70-180 mg/dL
时间窗: One month during each study period (sensor augmented pump and closed loop control)
Percentage of time of blood glucose in range 70-180 mg/dL as measured by the continuous glucose monitor.
次要结局
- Ecological Momentary Assessments(Assessments will be administered during the final 14 days of each study period (sensor-augmented pump and closed-loop control).)
- Sleep Patterns(Assessments will be made at baseline and at the end of each study SAP (4 weeks) and CLC (4 weeks).)
研究者
Sue Brown
Associate Professor
University of Virginia