Clinical Trials in South Korea / NCT06649162
Recruiting
Observational
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
NCT06649162 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Type 2 Diabetes
Study 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
Inclusion Criteria:
* 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 Criteria:
* 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.
Primary outcome measure(s)
- Percentage of subjects who correspond to high risk score (≥8) by evaluating simple NAFLD score — Baseline (visit 1)
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Andong Hospital | Andong | Gyeongsangbuk-do | Recruiting |
| Konkuk University medical center | Seoul | South Korea | Not Yet Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06649162 on ClinicalTrials.gov ↗ ← All trials in South Korea