SFlex_Netherland

Study Details

Study Design:

National, prospective, observational, multi-centre, investigator-initiated registry.

Schematic :

  1. Screening/Eligibility → ‘Real-world’ patient including, but not limited to, stable and unstable patients with single or multi-vessel disease and/or complex lesions.
  2. Planned follow-up → 12 months
  3. Endpoints
    1. Primary endpoint:
      • TLF at 12 months follow-up. TLF is defined as a composite endpoint comprising cardiac death, target vessel myocardial infarction (both Q-wave and non–Q-wave), or clinically driven TLR performed via either percutaneous or surgical methods.
    2. Secondary endpoints (12 months):
      • Overall stent thrombosis. 
      • All deaths (cardiac, vascular and non-cardiovascular). 
      • Any myocardial infarction (Q wave and non-Q wave MI).
      • Any repeat revascularization (target lesion and target vessel revascularization).
      • TVF: a composite endpoint of cardiac death, target vessel myocardial infarction, or clinically driven target vessel revascularization. 
      • MACE: a composite endpoint of cardiac death, myocardial infarction (Q wave and non-Q wave), emergent coronary bypass surgery, or repeat TLR (clinically driven/clinically indicated) by percutaneous or surgical methods. 

Abbreviation: TLF: Target Lesion Failure, TLR: Target Lesion Revascularization, TVF: Target Vessel Failure, MACE: Major adverse cardiac events

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