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Comparison of Liraglutide vs. Dulaglutide in type 2 diabetic outpatients using Flash Glucose monitoring (FGM)

Comparison of Liraglutide vs. Dulaglutide in type 2 diabetic outpatients using Flash Glucose monitoring (FGM) - Comparison of Liraglutide vs. Dulaglutide in type 2 diabetic outpatients using Flash Glucose monitoring (FGM)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030624
Enrollment
60
Registered
2017-12-28
Start date
2017-12-18
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes

Interventions

The CGM examination is carried out at least 14 days after administering liraglutide. Canagliflozin is changed to dulaglutide when the first CGM examination end. The CGM examination is carried out at l

Sponsors

Kitasato University School of Pharmacy
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients using Glucagon-Like Peptide 1 Receptor Agonist or the patients who judged a physician to need use of the Glucagon-Like Peptide 1 Receptor Agonist newly.

Exclusion criteria

Exclusion criteria: Patients with diabetic nephropathy more than stage 4 or with abnormal aspartate aminotransferase/alanine aminotransferase elevation (3 X the upper limit of normal) were excluded from this study.

Design outcomes

Primary

MeasureTime frame
Glycemic control is estimated as the mean blood glucose (MBG), the area under the glucose curve above 10.0mmol/L (area under the curve [AUC]>10), and the percentage of time above 10.0mmol/L (t>10).The AUC is calculated using the trapezoidal method. Intraday glycemic variability is assessed as the standard deviation (SD) and the mean amplitude of glycemic excursions (MAGE). Hypoglycemia, which is defined as a sensor value of <3.9mmol/L, was also calculated as a total time at <3.9mmol/L. Severe hypoglycemia is defined as a sensor value of <2.8mmol/L.

Countries

Japan

Contacts

Public ContactInoue Gaku

Kitasato University School of Pharmacy Center for Clinical Pharmacy and Clinical Sciences

inoueg@pharm.kitasato-u.ac.jp03-5791-6359

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026