The Prescription Patterns and Clinical Efficacy of Tenero Tab/Tenero M SR Tab

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age19+
SponsorHanlim Pharm. Co., Ltd.

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 volunteers

Qualifiers

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

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

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

Time frame
after 6 months of prescription for Tenero Tab/Tenero M SR Tab compared to baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.