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Table 1 Study schedule

From: A novel endothelial damage inhibitor for the treatment of vascular conduits in coronary artery bypass grafting: protocol and rationale for the European, multicentre, prospective, observational DuraGraft registry

 

Screening/ Enrolment

CABG/ hospital discharge

1 month

Annual follow-up (1–5 years)

Inclusion and exclusion criteria

X

   

Informed consent

X

   

Patient characteristics/medical history

X

   

EuroSCORE II

X

   

Procedural data

 

X

  

EQ-5D-5 L

X

  

X

Health economic data derived

  

X

X

MACCE

 

X

X

X

  1. MACCE Major adverse cardiac and cerebrovascular events (death, non-fatal myocardial infarction, repeat revascularisation, or stroke)