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Effect of Linagliptin on daily glucose excursion in Continuous Glucose Monitoring of Type2 diabetic patients

Effect of Linagliptin on daily glucose excursion in Continuous Glucose Monitoring of Type2 diabetic patients - L-CGM

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010880
Enrollment
100
Registered
2013-06-05
Start date
2013-07-01
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

Interventions

Group A
patients who take Linagliptin Group B
patients who take Voglibose

Sponsors

Japan society of Patient Reported Outcome
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with type 2 diabetes have not been taken antidiabetic medication more than 12 week. 2.7.4% and higher -HbA1c- under 10% (NGSP) at screening. 3.18 over - BMI under 30 4.eGFR,45 or higher 5.Twenty years of age or older, regardless of gender 6.Written consent for participation in the study

Exclusion criteria

Exclusion criteria: 1.Type 1 and secondary diabetes 2.Severe infectious disease, before or after surgery, and severe trauma 3.Events of myocardial infarction, cerebral stroke, cerebral infarction and TIA in the past 3 month. 4.Moderate or severer heart failure(NYHA/New York Heart Association stage III or severer) 5.Severe liver dysfunction (ALT,AST and ALP face 3 times the normal level) 6.Past medical history of hypersensitivity to investigational drugs. 7.Patients addicted to alcohol and drugs. 8.Pregnant, lactating, and possibly pregnant women and those planning to become pregnant. 9.Patients with cancer. 10.Patent receiving steroid therapy with inflammatory affection. 11.Past medical history of abdominal operation and ileus. 12.Judged as ineligible by clinical investigators.

Design outcomes

Primary

MeasureTime frame
Change of mean 24 hours glucose level at the point of 12 weeks from Baseline

Countries

Japan

Contacts

Public ContactHiroki Takyama

Soiken.inc Division of clinical study support

takayama@soiken.com03-3295-1350

Outcome results

None listed

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