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Recruiting Not applicable

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

NCT05149625 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2022-11-27
Last updated
2023-04-12

Condition(s) studied

Diabetes Mellitus

Investigational drug(s) / intervention(s)

Dexcom G6

Dexcom G6: continuous glucose monitoring device

Study summary

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.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Patients over 19 years of age * Preoperative diabetes history * Patients who underwent subtotal or total pancreatectomy * Patients who were diagnosed with diabetes mellitus in the evaluation of endocrine function test on the 7th day after pancreaticoduodenectomy, central pancreatectomy, or distal pancreatectomy Exclusion Criteria: * Patients who have used continuous blood glucose measurement device more than once before. * Elderly patients who are not accustomed to using the smartphone applications * Serious systemic diseases that can affect diabetes (chronic kidney disease, heart failure, decompensated liver cirrhosis, etc.) * Steroid user during the study period * Major medical or psychiatric condition that will affect response to treatment

Primary outcome measure(s)

  • Hemoglobin A1c (HbA1c) — postoperative 3months

Trial sites (1)

FacilityCityRegionStatus
Department of Surgery, Seoul National University College of Medicine Seoul South Korea Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05149625 on ClinicalTrials.gov ↗ ← All trials in South Korea