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Continuous glucose monitor use after hospital discharge in insulin-treated type 2 diabetes

Compares a real-time glucose sensor with finger-stick checks in adults with type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Effects of Real-time Continuous Glucose Monitoring System on Hospital-to-home Transitional Blood Glucose Control

Key facts

Where
Shanghai, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT06591286, who can take part

Where in China

  • Shanghai 6th People's HospitalShanghai, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Shanghai 6th People's Hospital
Trial code
NCT06591286
Record updated
29 November 2024
Original description
Glucose monitoring is an important part of self-management for patients with diabetes. The results of glucose monitoring not only help to assess the degree of glucose metabolism disorders in patients, but also help physicians to make clinical decisions and guide patients in self-management. Despite extensive efforts and advances in diabetes management during hospitalization, glucose control after patients is discharged home remains a challenge. This trial aims to explore the effect of real-time continuous glucose monitoring (RT-CGM) system compared to self-monitoring of blood glucose (SMBG) group on glucose and self-efficacy of type 2 diabetes patients treated with insulin after discharge from the hospital.Read full original descriptionShow less

Effects of Real-time Continuous Glucose Monitoring System on Hospital-to-home Transitional Blood Glucose Control and Self-efficacy Among Patients With Type 2 Diabetes Treated With Insulin

Glucose monitoring is an important part of self-management for patients with diabetes. The results of glucose monitoring not only help to assess the degree of glucose metabolism disorders in patients, but also help physicians to make clinical decisions and guide patients in self-management. Despite extensive efforts and advances in diabetes management during hospitalization, glucose control after patients is discharged home remains a challenge. This trial aims to explore the effect of real-time continuous glucose monitoring (RT-CGM) system compared to self-monitoring of blood glucose (SMBG) group on glucose and self-efficacy of type 2 diabetes patients treated with insulin after discharge from the hospital.

Inclusion: 18 years old ≤ age ≤ 80 years old; Type 2 diabetes admitted to Department of Endocrinology and Metabolism; 8% ≤ HbA1c ≤ 12% in the last 1 month; Insulin therapy within 1 month of planned discharge from hospital; Frequency of self-monitoring of blood glucose <4 times per week and no use of real-time continuous glucose monitoring system in the 3 months prior to hospitalisation; Willing and able to provide written informed consent and comply with the requirements of this study.

Exclusion: Oral steroid hormone therapy; Patients with acute complications of diabetes (including Diabetic ketoacidosis, hyperglycemia and hyperosmolality, Lactic acidosis); Patients with severe liver disease (alanine aminotransferase or glutamine aminotransferase exceeding more than three times the upper limit of normal); Participants were unable to tolerate tape adhesive around sensor placement area, or with medically documented allergy towards the adhesive (glue) of plasters, or with serious skin diseases (e.g. psoriasis vulgaris, bacterial skin diseases) around sensor placement area; Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study; Patients with severe kidney injury or end-stage renal disease (eGFR < 30 mL/min/1.73 m2); Pregnant, breastfeeding, women of childbearing age who are unwilling to use contraception during the study period.

ClinicalTrials.gov NCT06591286