RecruitingNCT05970237

A Study to Evaluate the Efficacy and Safety of Dapagliflozin in Patient With Type 2 Diabetes Mellitus and Hypertension

A Multicenter, Prospective, Non-interventional, Observational Study to Evaluate the Efficacy and Safety of Dapagliflozin in Patient With Type 2 Diabetes Mellitus and Hypertension


Sponsor

Boryung Pharmaceutical Co., Ltd

Enrollment

9,000 participants

Start Date

Jul 26, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this clinical trial is to evaluate the efficacy and safety of dapagliflozin in patient with type 2 diabetes mellitus and hypertension


Eligibility

Min Age: 19 Years

Inclusion Criteria3

  • Those diagnosed with type 2 diabetes mellitus accompanied by hypertension who are scheduled to be administrated Trudapa Tab. or Trudapa M SR Tab.
  • Those who voluntarily signed a written personal information agreement to participate in this clinical study.
  • Those able to understand this study, be cooperative in the execution of the study, and participate in the study until its completion.

Exclusion Criteria4

  • Patients with secondary hypertension: Secondary hypertension is not limited to the following diseases; (e.g., coarctation of the aorta, hyperaldosteronism, renal artery stenosis, pheochromocytoma, Cushing's syndrome and polycystic kidney disease, etc.)
  • Those who have a history of taking dapagliflozin within 4 weeks of baseline (Visit 1)
  • Those who are expected to need insulin prescription during the study period
  • Pregnant women, breast-feeding women

Locations(1)

Gachon University Gil Medical Center

Incheon, Namdong-gu, South Korea

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NCT05970237


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