Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
Healthy Volunteers
NCT05149625

Comparison of the Efficacy and Satisfaction of Blood Glucose Management Between Continuous Glucose Monitoring Versus Traditional Self-blood Glucose Measurement in Diabetic Patients After Pancreatectomy

Led by Seoul National University Hospital · Updated on 2023-04-12

172

Participants Needed

1

Research Sites

213 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare the efficacy and satisfaction of blood glucose management between continuous glucose monitoring versus traditional self blood glucose measurement in diabetic patients after pancreatectomy.

CONDITIONS

Official Title

Comparison of the Efficacy and Satisfaction of Blood Glucose Management Between Continuous Glucose Monitoring Versus Traditional Self-blood Glucose Measurement in Diabetic Patients After Pancreatectomy

Who Can Participate

Age: 19Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 19 years of age
  • History of diabetes before surgery
  • Patients who underwent subtotal or total pancreatectomy
  • Diagnosis of diabetes mellitus based on endocrine function test 7 days after pancreatectomy
Not Eligible

You will not qualify if you...

  • Previous use of continuous blood glucose monitoring device more than once
  • Elderly patients not familiar with smartphone applications
  • Serious systemic diseases affecting diabetes such as chronic kidney disease, heart failure, or decompensated liver cirrhosis
  • Use of steroids during the study period
  • Major medical or psychiatric conditions affecting treatment response

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Surgery, Seoul National University College of Medicine

Seoul, South Korea, 110-744

Actively Recruiting

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Research Team

J

Jin-Young Jang, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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