Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

ENAVOgliflozin Outcome Trial in Patients With Severe Aortic Stenosis After Transcatheter Aortic Valve Replacement

The goal of this trial is to to determine whether use of a novel SGLT2 inhibitor, Enavogliflozin 0.3 mg once daily is superior to placebo, when added to standard-of-care, in reducing the composite of major cardiovascular events and Heart Failure events (hospitalization for Heart Failure or urgent Heart Failure visit) among patients who underwent transcatheter aortic valve replacement for severe aortic stenosis and with heart failure with preserved ejection fraction.

Participants needed: 1,040
Trial details
Phase: Phase 4Age: 19+Biological sex: AllType: InterventionalSponsor: Duk-Woo Park, MDUpdated: Jun 29, 2026Locations: 31
Eligibility criteria

correct positioning of a single prosthetic heart valve into the proper anatomica... [+5]

Acute decompensated Heart Failure (exacerbation of chronic Heart Failure) requir... [+24]

Status: Recruiting

Evaluation of Effectiveness and Safety of Ultimaster™ Tansei™ Stent and/or Ultimaster Nagomi™ Stent in Routine Clinical Practice

This study is to evaluate the effectiveness and safety of Ultimaster Tansei stent and/or Ultimaster Nagomi stent in the "real-world" daily practice.

Participants needed: 2,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Duk-Woo Park, MDUpdated: Jun 26, 2026Locations: 11
Eligibility criteria

Patients ≥ 19 years old [+2]

Patients with a mixture of other drug-eluting stents (DESs) [+2]

Status: Recruiting

Potassium-Competitive Acid Blocker Versus pROton-Pump Inhibitor for GastroproTECTion Strategies In Patients at High Gastro-Intestinal Bleeding Risk Receiving Antithrombotic Therapy

The primary aim of this study is to evaluate the efficacy and safety of novel P-CAB (tegoprazan 50 mg once daily) as compared with standard PPI (rabeprazole 20 mg once daily) for protection of GI events in patients with known cardiac and vascular disease receiving chronic use of antithrombotic drugs (either antiplatelets, OAC, and its combinations) who are at high GI bleeding risk. The primary hypothesis is that P-CAB (experimental arm) would non-inferior to PPI (standard arm) with respect to the rate of the primary composite end point of GI events at 12 months after randomization.

Participants needed: 3,320
Trial details
Phase: Phase 4Age: 19+Biological sex: AllType: InterventionalSponsor: Duk-Woo Park, MDUpdated: Jun 26, 2026Locations: 45
Eligibility criteria

Patients 19 years of age or older with known cardiac and vascular disease who ar... [+8]

Active bleeding at the time of inclusion or a history of hereditary or acquired... [+21]

Status: Recruiting

Diabetes-Centered Evaluation of Revascularization Strategy of Functional and Imaging-CombiNEd State-of-the-Art Percutaneous Coronary Intervention or Coronary-Artery Bypass Grafting in Patients With Diabetes Mellitus and Multivessel Coronary Artery Disease

The objective of this randomized study was to compare outcomes of imaging-and physiology-guided state-of-the-art percutaneous coronary intervention (PCI) to coronary artery bypass grafting (CABG) in patients with diabetes and three-vessel CAD (not involving left main).

Participants needed: 1,500
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Duk-Woo Park, MDUpdated: Jun 24, 2026Locations: 39
Eligibility criteria

The subject must be ≥20 years of age with angina and/or evidence of myocardial i... [+3]

Unprotected left main coronary artery disease. [+15]

Status: Recruiting

Transpacific TAVR Registry

This registry evaluates the long-term outcome of Transcatheter aortic valve replacement (TAVR) in real-world clinical practice.

Participants needed: 10,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Duk-Woo Park, MDUpdated: Jan 2, 2026Locations: 7
Eligibility criteria

All patients undergoing TAVR [+1]