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Clinical Trials/KCT0006914
KCT0006914
Recruiting
未知

Comparison of clinical outcomes between non-polymer drug-coated stent versus ultrathin strut biodegradable polymer drug-eluting stent in patients undergoing percutaneous coronary intervention: SMART-CHOICE 4 randomized trial

Samsung Medical Center0 sites3,000 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Samsung Medical Center
Enrollment
3000
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\)Subject must be at least 19 years of age
  • 2\)Subject who is able to understand risks, benefits and treatment alternatives and sign informed consent voluntarily.
  • 3\)Patients with at least one lesion with equal or greater than 50% diameter stenosis requiring treatment with drug\-eluting stents (DES) in native coronary artery or graft

Exclusion Criteria

  • 1\)Patients unable to provide consent
  • 2\)Patients with known intolerance major components of drug\-eluting stents
  • 3\)Patients who have non\-cardiac co\-morbid conditions with life expectancy \<1 year or that may result in protocol non\-compliance (per site investigator’s medical judgment)
  • 4\)Pregnant or lactating women
  • 5\) patient with hemodynamic instability or psychogenic shock

Outcomes

Primary Outcomes

Not specified

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