Clinical Trials in South Korea / NCT05970237
Recruiting
Observational
A Study to Evaluate the Efficacy and Safety of Dapagliflozin in Patient With Type 2 Diabetes Mellitus and Hypertension
NCT05970237 · tracked via the Priya Life Science South Korea tracker
Condition(s) studied
Diabetes MellitusHypertension
Study 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
Inclusion Criteria:
* 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 Criteria:
* 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
Primary outcome measure(s)
- Target blood pressure control rate — 12weeks after administration
- Target blood glucose achievement rate — 12weeks after administration
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Gachon University Gil Medical Center | Incheon | Namdong-gu | Recruiting |
More Boryung Pharmaceutical Co., Ltd trials in South Korea
Other trials for the same condition
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CART-BP Prospective Study for Hypertension Control
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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 NCT05970237 on ClinicalTrials.gov ↗ ← All trials in South Korea