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A randomized and comparative study of DPP4 inhibitors versus SGLT2 inhibitors using cotinuous glucose monitoring (CGM)

A randomized and comparative study of DPP4 inhibitors versus SGLT2 inhibitors using cotinuous glucose monitoring (CGM) - A randomized and comparative study of DPP4 inhibitors versus SGLT2 inhibitors using cotinuous glucose monitoring (CGM)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015087
Enrollment
20
Registered
2014-09-08
Start date
2014-09-08
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Type 2 diabetes mellitus

Interventions

SGLT2 inhibitors: This study to examine the change in SD of 24h and MAGE by CGM,blood glucose levels,Body weight,urine volume before and after the start. DPP-4 inhibitors: This study to examine the

Sponsors

Yokohama City University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)before test registration - the meal and exercise cure for one month or more or a meal and an exercise cure, and diabetic medicine and inpatient 2)HbA1c(NGSP):more than 7.0%, less than 14.0% 3)126mg/dl<=FPG<250mg/dl and 200mg/dl<=PPG<350mg/dl 4)eGFR more than 45ml/min/1.73m 2 5)Type 2 diabetes 6)Pts with written IC 7)Age more than 20, less than 85

Exclusion criteria

Exclusion criteria: 1)severe ketosis, diabetic coma within 6 months 2)severe infection, before operation, severe trauma 3)severe hepatic dysfunction 4)or severe renal dysfunction (Cr: more than 1.5mg/dl) 5)Patients who use of insulin 6)pregnacy 7)Allergy for sitagliptin, nateglinide,liraglutide and exenatide 8)Patients judged by the investigator to be ineligible for some other reason

Design outcomes

Primary

MeasureTime frame
SD of blood glucose by CGM

Secondary

MeasureTime frame
1)averate blood glucose, MAGE by CGM 2)FPG and PPG at 1, 2, 3, 4, 5, 6, 7 days of treatment 3)%chagne of FPG, HbA1c,IRI,CPR, a from baseline 4)a questionnaire survey

Countries

Japan

Contacts

Public ContactJoe Nagakura

Yokohama City University Medical Center Department of Endocrinology and Diabetes

jo0806nagakura@hotmail.com045-261-5656

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026