NCT04901143已完成不适用
Meal Handling of Advanced Closed Loop Insulin Delivery.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
- 试验地点
- 1
- 主要终点
- Time in range
研究概览
简要总结
The study will Compare meal related glycemic indices following 2 types of meal announcement:
- Conventional assessment of carb content plus carb equivalence of proteins and fat
- Algorithm device optimal universal meal announce equivalent
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
- 20 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subject is 20 to 70 years of age at time of screening
- •Subject's weight is between 50 and 120 kg
- •A clinical diagnosis of Type 1 diabetes as determined by the Investigator for a minimum of 36 months prior to enrollment
- •Subject has ongoing use of an insulin pump and rtCGM ≥ 6 months prior to screening
- •current use of 670G 4.0 pump
- •Subject has an A1C value ≤ 10.0% demonstrated at the time of enrollment.
- •Subject uses a rapid-acting analogue insulin in his/her pump
- •Patient is willing to undergo all study procedures
- •English proficiency
- •Minimum daily insulin requirement (Total Daily Dose) of greater than or equal to 8 units
排除标准
- •Female subject who has a positive serum pregnancy screening test, or who plans to become pregnant during the course of the study
- •Subject has unresolved adverse skin condition, or unable to tolerate tape adhesive, in the area of sensor placement or device replacement (e.g., psoriasis, rash, Staphylococcus infection)
- •Subject has a history of hypoglycemic seizure or hypoglycemic coma within the past 12 months
- •Subjects currently taking adjunct therapy with SGLT2-inhibitors, Amylin.
- •Subject has a history of seizure disorder unrelated to diabetes within the past 12 months
- •Gastroparesis, uncontrolled thyroid disorder, Addison disease,. , Pituitary insufficiency
- •Subject has a history of myocardial infarction, unstable angina, coronary artery bypass surgery, coronary artery stenting, transient ischemic attack (TIA), cerebrovascular accident (CVA), congestive heart failure, ventricular rhythm disturbances, or thromboembolic disease within the past 6 months
- •Subject has a presence of a cardiac pacemaker or any other device that may be sensitive to radio frequency telemetry
- •Subject has any condition, including screening lab values that in the opinion of the Investigator may preclude him/her from participating in the study and completing study related procedures
- •Subject is actively participating in other investigational study (drug or device)
- •Subjects who consume alcohol daily
- •Use of CGM (other than per protocol) throughout the duration of the study
- •Use of Hydroxyurea medication
结局指标
主要结局
Time in range
时间窗: 300 minutes
AUC glucose 300 minutes post meal
次要结局
未报告次要终点
研究者
Prof. Amir Tirosh
Prof. Amir Tirosh
Sheba Medical Center
研究点 (1)
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