RecruitingNCT06649162

A Study to Identify the Risk of Non-alcoholic Fatty Liver Disease (NAFLD) in Patients With Type 2 Diabetes in Clinical Practice and to Evaluate the Clinical Usefulness of Dapagliflozin/Pioglitazone Combination Therapy

A Multi-center, Prospective, Cohort Study to Identify the Risk of Non-alcoholic Fatty Liver Disease (NAFLD) in Patients With Type 2 Diabetes in Clinical Practice and to Evaluate the Clinical Usefulness of Dapagliflozin/Pioglitazone Combination Therapy


Sponsor

Boryung Pharmaceutical Co., Ltd

Enrollment

10,000 participants

Start Date

Sep 30, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to identify the risk of non-alcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes in clinical practice and to evaluate the clinical usefulness of Dapagliflozin/Pioglitazone combination therapy


Eligibility

Min Age: 19 Years

Inclusion Criteria2

  • Among patients with type 2 diabetes, those who are scheduled to administer a fixed-dose combination of dapagliflozin/pioglitazone at baseline (visit 1)
  • Those who voluntarily signed a written personal information collection and usage agreement after listening to an explanation about the objective and method, etc. of this clinical study.

Exclusion Criteria2

  • Those who have a history of taking a fixed-dose combination of dapagliflozin/pioglitazone at baseline (visit 1).
  • Those who are expected to need insulin prescription during the study period.

Locations(2)

Andong Hospital

Andong, Gyeongsangbuk-do, South Korea

Konkuk University medical center

Seoul, South Korea

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NCT06649162


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