Insulin Titration System Based on Deep Learning

Fudan University

Status

Completed

Conditions

Diabetes Mellitus Type 2 - Insulin-Treated

Treatments

Device: Insulin Titration System

Study type

Interventional

Funder types

Other

Identifiers

NCT05409391

ZSE-202205

Details and patient eligibility

About

This is an open-labeled, one-arm intervention trial to access the effect and safety of the Insulin Titration System Based on Deep Learning in patients with Type 2 Diabetes Mellitus.

Full description

The study enrolls 13 patients with Type 2 Diabetes in Zhongshan Hospital who are on treatment with insulin. After screening for the inclusion and exclusion criteria, eligible patients will receive insulin dosage titration set by the Insulin Titration System Based on Deep Learning in the intervention trial. The goal of insulin therapy was to achieve preprandial capillary blood glucose between 5.6-7.8 mmol/L and postprandial capillary glucose less than 10.0mmol/L. All patients are studied for 5 consecutive days or untill hospital discharge. For each patient, capillary glucose concentration was measured at 7 time points of fasting, after breakfast, before and after lunch, before and after dinner, and before bedtime a day using Glucometer (Glupad, Sinomedisite, China). Capillary glucose measurements were performed by the nurse staff according to standard procedures with a point-of-care testing device, which is integrated into the HIS system. And continuous glucose monitoring (CGM) was performed using flash glucose monitoring (Abbott Freestyle Libre, USA) placed on the upper left arm. This study will be conducted in the Department of Endocrinology, Zhongshan Hospital,Fudan University.

Enrollment

16 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

type 2 diabetes
age of 18-75 years
HbA1c between 7.0% and 11.0%.

Exclusion criteria

subjects with acute complications of diabetes, such as ketoacidosis or hyperglycemic hyperosmolar state;
BMI ≥ 45kg/m2;
women who are pregnant or breast-feeding;
subjects with severe cardiac, hepatic, renal diseases; subjects with any psychiatric or psychological diseases;
subjects with severe edema, infections or peripheral circulation disorders, receiving surgery during hospitalization;
subjects who could not comply with the protocol