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NCT06591286Recruiting

Effects of Real-time Continuous Glucose Monitoring System on Hospital-to-home Transitional Blood Glucose Control

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

Source: ClinicalTrials.gov · Last updated 29 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
7 Sept 2024
Start date
25 Oct 2024
Primary completion date
10 Mar 2026
Lead sponsor
Shanghai 6th People's Hospital
NCT number
NCT06591286

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 25 Oct 2024 to the primary completion date, 10 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Oral steroid hormone therapy.

Other illness

  • 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.

Lab values

  • Patients with severe kidney injury or end-stage renal disease (eGFR \< 30 mL/min/1.73 m2).

Age

  • Pregnant, breastfeeding, women of childbearing age who are unwilling to use contraception during the study period.

Who the study is looking for

  • 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.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shanghai 6th People's Hospital
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ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.