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Clinical Trials/KCT0003325
KCT0003325
Completed
未知

Optical CoherenCe tomography-gUided coronary intervention in Patients with complex lesIons: a randomized controlled trial (OCCUPI trial)

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Yonsei University Health System, Severance Hospital
Enrollment
1604
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
February 5, 2024
Last Updated
2 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 19\-85 years
  • \- Patients with ischemic heart diseases (including stable angina, unstable angina and acute myocardial infarction) presented with typical chest pain or objective evidences of myocardial ischemia (positive invasive or non\-invasive studies,
  • electrocardiogram (ECG) consistent with ischemia, or elevated cardiac enzymes)
  • \- Complex coronary stenotic lesions (\>50% based on visual estimate) considered for coronary revascularization with DES
  • \- Definition of complex lesions (at least one):
  • ? Acute myocardial infarction
  • ? Chronic total occlusion
  • ? Long lesion: expected stent length \=28mm based on angiographic estimation
  • ? Calcified lesion
  • ? Bifurcation (including all techniques, one\- or two\-stent)

Exclusion Criteria

  • \- Severe hepatic dysfunction (\=3 times normal reference values)
  • \- Significant renal dysfunction (Serum creatinine \>2\.0 mg/dL)
  • \- Platelet count \<100,000 cells/mm3 or \>700,000 cells/mm3, a white blood cell count of \<3,000 cells/mm3, hemoglobin \<8\.0 g/dL, or other known bleeding diathesis
  • \- Hemodynamically unstable during procedures or cardiogenic shock
  • \- Pregnant women or women who might be pregnant
  • \- Life expectancy; less than 1 year
  • \- Inability to understand or read the informed content

Outcomes

Primary Outcomes

Not specified

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