A Control-IQ Technology 2.0 Feasibility Study in Adult and Adolescent Subjects
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 66
- 试验地点
- 2
- 主要终点
- Significant Hypoglycemia
研究概览
简要总结
The purpose of this study is to obtain preliminary safety and performance data on planned improvements to Control-IQ technology.
详细描述
This feasibility study is a prospective, single arm, single center study with a run-in phase, followed by a 48-hour supervised phase, followed by a 4-week at home study with sequential interventions (new feature use). Approximately 30 subjects, both male and female, aged 14 and up, will participate in the study, using new features each week with the t:slim X2 insulin pump with Control-IQ technology.
The first 5 subjects in the study will complete a 48 hour session with multiple challenges during use of Control-IQ technology 2.0, before moving on the outpatient portion of the trial.
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
- 14 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult and adolescent male and female subjects >age 14 years
- •Clinical diagnosis of Type 1 diabetes for at least one year
- •Experienced Control-IQ technology user for ≥3 months.
- •Use of Control-IQ technology in closed-loop at least 80% of the 2-week time period before screening.
- •Not pregnant or planning a pregnancy during the time period of the study
- •Using only Humalog U-100 or Novolog U-100 insulin
- •ICR and ISF optimized per investigator judgement
- •CGM time in range (70-180 mg/dL) at least 50% on Control-IQ technology
- •Has current glucagon product to treat severe hypoglycemia (injectable or nasal) at home (will provide prescription if they do not have one)
- •Willing to:
- •Share Dexcom G6 CGM data with study staff and Tandem
- •Share t:connect data with Tandem
- •Eat meals with known carbohydrate amounts
- •Take meal boluses as directed (use of different options as scheduled and instructed)
- •Follow study Glycemic Treatment Guidelines for hypo and hyperglycemia
- •Keep food and exercise diary
- •Set accurate sleep schedule on pump
- •Exercise while using exercise activity in Control-IQ technology at least twice weekly
- •Complete questionnaires before and after using investigational device
- •Sign an informed consent form
- •Willingness to use the Dexcom G6 app on their personal phone throughout the study, and share real time CGM information with a local contact and study staff
- •Availability of a local contact who has access to the study participant, knows their whereabouts, and agrees to be promptly available if contacted by study staff. If the subject lives alone, the local contact must live within 30 minutes and have access to the subject overnight.
排除标准
- •Diabetic ketoacidosis (DKA) in the past 6 months
- •Severe hypoglycemia (needing assistance) in the past 6 months
- •Inpatient psychiatric treatment in the past 6 months
- •History of drug abuse (defined as any illicit drug use) or history of alcohol abuse prior to screening or is unwilling to agree to abstain from illicit drugs throughout the study
- •History of heart, lung or kidney disease determined by the investigator to interfere with the study
- •Use of glucocorticoids, beta blockers or other medications determined by investigator to interfere with the study
- •Use of long-acting insulin or any non-insulin glucose lowering agents (i.e. SGLT-2 inhibitor) other than metformin
- •Use of Afrezza during the study period
- •Febrile illness within 3 days of the start of the study
- •Subject is pregnant or lactating or intending to become pregnant before or during participation in this study
- •For subjects >50 years old or with diabetes duration >20 years who will be exercising as part of the 48 hour study, abnormal electrocardiogram consistent with increased risk of arrhythmia, ischemia, or prolonged QTc interval (> 450 ms)
- •Significant chronic kidney disease (eGFR < 60) or hemodialysis
- •Significant liver disease
- •History of adrenal insufficiency
- •History of abnormal TSH consistent with hypothyroidism or hyperthyroidism that is not appropriately treated
研究组 & 干预措施
Control-IQ 2.0 technology 2.0 on the t:slim X2 insulin pump
After a run-in week, each subject will use different combinations of new features of the system each week, in random order, for 4 weeks, using the t:slim X2 insulin pump with Control-IQ technology 2.0.
The first 5 subjects participated in a 48-hour supervised hotel phase before continuing in the outpatient setting.
干预措施: Control-IQ technology 2.0 (Device)
结局指标
主要结局
Significant Hypoglycemia
时间窗: 8 weeks
CGM percent time \<54 mg/dL during each week of feature use, as well as during baseline and run-in periods
Diabetic Ketoacidosis
时间窗: 8 weeks
Number of participants with Diabetic Ketoacidosis (per protocol) during each week of feature use, as well as during baseline and run-in periods
Severe hypoglycemia (needing assistance)
时间窗: 8 weeks
Number of severe hypoglycemic events (per protocol) during each week of feature use, as well as during baseline and run-in periods
Serious Adverse Events
时间窗: 8 weeks
Number of Serious Adverse Events during each week of feature use, as well as during baseline and run-in periods
次要结局
- Percent of time 70-180 mg/dL(8 weeks)
- CGM Metrics by time of day(8 weeks)
- Percent of time <70 mg/dL(8 weeks)
- Percent of time > 250 mg/dL(8 weeks)
- Percent of time 70-140 mg/dL(8 weeks)
- Postprandial glycemic peak mg/dL(8 weeks)