Clinical Application of an Open-source Artificial Pancreas System in Adult Inpatients With Diabetes

Artificial Pancreas (AP), as the treatment of type 1 diabetes, has attracted more and more attention in recent years. The artificial pancreas system is an Automatic Insulin Delivery/AID device that consists of three main elements: The Continuous Glucose Monitoring , insulin pump and central algorithm control system ,it can automatically calculate the immediate insulin infusion dose according to the immediate blood glucose, giving continuous subcutaneous infusion, and maximizing the simulation of the physiological secretion pattern of human insulin, so as to achieve closed-loop blood glucose management. Compared with traditional insulin pump therapy , artificial pancreas system has advantages such as higher intelligence, more stable blood glucose control, and less burden of blood glucose management. While greatly improving patients' quality of life, its safety has also been verified in a number of foreign clinical studies.

Inclusion criteria

• Age is 18~75 years old (including 18 years old and 75 years old), gender is not limited;
• Patients with type 1 diabetes mellitus (T1DM);
• Patients with type 2 diabetes mellitus (T2DM) who require insulin therapy;
• Those who sign the informed consent form and voluntarily participate in this clinical trial;
• Be able to understand the trial and cooperate with the test procedure, and be able to follow up the observer as required.

Exclusion criteria

• Patients who are not suitable for insulin pump therapy;
• Acute complications of diabetes, such as diabetic ketoacidosis, diabetic hyperosmolar non-ketotic coma;
• Hyperglycemia with severe circulatory disorders and patients with shock;
• Cardiac function grade III or above; ALT or AST exceeds the upper limit of normal value by more than 3 times; Serum creatinine more than 442μmol/L; Hemoglobin less than 90g/L; White blood cell count < 4.0×109/L or platelet count <90×109/L;
• Those who are allergic to adhesive tape;
• Patients with skin diseases such as rash and prurigo, or abnormal coagulation function;
• Women who are pregnant or lactating, or those who have a family plan during clinical trials;
• Those who suffer from mental illness, have no self-control, and cannot express themselves clearly;
• Those who have participated in clinical studies of other drugs, biologics or medical devices before screening but have not reached the time limit of the primary research endpoint;
• Other circumstances that participants deems inappropriate to participate in the clinical trial.