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Observational Study Gemigliptin in Patients Aged ≥ 65 Years With Type 2 Diabetes Mellitus

Conditions
Type 2 Diabetes Mellitus
Registration Number
NCT05281029
Lead Sponsor
LG Chem
Brief Summary

The aim of this study is to evaluate safety and effectiveness of treatment with gemigliptin for 24 weeks in Korean patients aged ≥ 65 years with type 2 diabetes mellitus in routine clinical settings

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
3000
Inclusion Criteria
  • Patients who have been started on gemigliptin in accordance with the approved label and who have signed on the consent form
Exclusion Criteria
  • Patients with previous exposure to gemigliptin and current participation in clinical trials

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change from Baseline of HbA1c at 24 weeksBaseline, 24 weeks
Secondary Outcome Measures
NameTimeMethod
Change from Baseline of HbA1c at 12 weeksBaseline, 12 weeks
The rate of subjects who reached the target value of less than 7% (reasonable HbA1c goal) of HbA1c.24 weeks

Trial Locations

Locations (1)

Severance Hospital

🇰🇷

Seoul, Korea, Republic of

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