Evaluation of the DreaMed Advisor Pro System in Subjects With Type 1 Diabetes Treated With Multiple Daily Injections of Insulin
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 35
- 试验地点
- 1
- 主要终点
- Percentage of readings below 54 mg/dl
研究概览
简要总结
A multi center, open label, prospective study that will include up to 100 subjects with Type 1 Diabetes treated with Multiple Daily Injections (MDI) of insulin according to a predefined sliding scale plan or carbohydrate ratio (CR) and correction factor (CF) plan, and Self-Monitoring of Blood Glucose (SMBG) or Continuous Glucose Monitoring (CGM).
The study will include screening, a 3-4 weeks run-in period and a 6 weeks intervention period. Subjects will be asked to record their insulin delivery during basal/bolus insulin treatment (using dedicated apps and/or connected pens) and their daily activities (meals, physical activity etc.) using electronic log (implemented on Dedicated Apps), for a total period of 9-10 weeks.
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 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Documented T1D for at least 1 year prior to study enrolment
- •Subjects aged 18 - 65 years old
- •A1c at inclusion ≤ 10%
- •Subjects using basal-bolus MDI therapy:
- •Basal insulin: Glargine, Degludec, or Determir
- •Bolus insulin: regular insulin, rapid analogues or ultra-rapid analogues
- •Subjects using CGM or SMBG that are compatible with data transmission to the study DMS.
- •BMI < 28 kg/m2
- •Subjects willing to follow study instructions:
- •For SMBG users: measure capillary blood glucose at least 4 times a day and twice a week 7-point profile (optional). Document blood glucose level, insulin delivery, meals and daily activities. Wear blinded CGM.
- •For CGM users: Use CGM according to manufacture instructions, Document insulin delivery, meals and daily activities.
- •Subjects have connection to the internet at home.
- •Subjects have a smartphone compatible with study requirements
- •Subjects willing and able to sign a written informed consent form.
排除标准
- •An episode of diabetic keto-acidosis within the month prior to study entry and/or severe hypoglycemia resulting in seizure or loss of consciousness in the month prior to enrolment.
- •Concomitant diseases/ treatment that influence metabolic control or any significant diseases /conditions including psychiatric disorders and substance abuse that in the opinion of the investigator is likely to affect the subject's ability to complete the study or compromise patients' safety
- •Relevant severe organ disorders (diabetic nephropathy, diabetic retinopathy, diabetic foot syndrome) or any secondary disease or complication of diabetes mellitus, such as:
- •Subject has unstable or rapidly progressive renal disease or is receiving dialysis
- •Subject has active proliferative retinopathy
- •Active gastroparesis
- •Participation in any other interventional study
- •Female subject who is pregnant or planning to become pregnant within the planned study duration
- •Subject is in the "honeymoon" phase - i.e. less than 0.5 insulin units/kg per day.
- •Drug or alcohol abuse.
研究组 & 干预措施
Intervention
Subject's glucose and insulin data will be transferred to the DreaMed Advisor Pro system. Optimization of insulin treatment plan will be done using the DreaMed Advisor Pro algorithm. After approval by the study physician (may override the suggestions for safety reasons), the treatment plan will be sent to the subject to be followed for the following 3 weeks. The study team will follow-up with a phone call to the subject to verify the subject received the updated treatment plan.
干预措施: Advisor Pro (Device)
结局指标
主要结局
Percentage of readings below 54 mg/dl
时间窗: 9 weeks
Compare percentage of readings below 54 mg/dl during 3 weeks run-in period to percentage of readings below 54 mg/dl during intervention period.
次要结局
- Percentage of readings within range of 70-180 mg/dl(9 weeks)
- Change in HbA1C post study treatment(9 weeks)