About this trial
This study is to observe the prescription patterns and clinical efficacy of patients prescribed with Tenero Tab/Tenero M SR Tab for diabetes treatment in routine clinical practice.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults over 19 years of age
Individuals diagnosed with type 2 diabetes.
Individuals who, at the clinical discretion, are prescribed Tenero Tab or Tenero M SR Tab for the purpose of diabetes treatment for the first time.
Individuals who have voluntarily provided written consent to participate in this study.
Disqualifiers
Pregnant or breastfeeding women.
Individuals who are contraindicated according to the approved indications of Tenero Tab/Tenero M SR Tab.
Other cases where the principal investigator and study personnel deem individuals ineligible for participation in this clinical trial.
Trial population
Patients prescribed Tenero Tab/Tenero M SR Tab for diabetes treatment.
Trial design
Case-only
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Change in HbA1c at 6 months of prescribing Tenero Tablet/Tenero Emextended Release Tablet compared to baseline
Change in HbA1c at 6 months of prescribing Tenero Tablet/Tenero Emextended Release Tablet compared to baseline
Sponsors and contacts
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