跳至主要内容
临床试验/NCT06649162
NCT06649162招募中不适用

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

Boryung Pharmaceutical Co., Ltd2 个研究点 分布在 1 个国家目标入组 10,000 人开始时间: 2024年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
10,000
试验地点
2
主要终点
Percentage of subjects who correspond to high risk score (≥8) by evaluating simple NAFLD score

研究概览

简要总结

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

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

Percentage of subjects who correspond to high risk score (≥8) by evaluating simple NAFLD score

时间窗: Baseline (visit 1)

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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