cardiovascular disease coronary artery disease
Conditions
Interventions
Patients who are participating in this study are randomized in two groups. In
both groups The wounds wil be closed with a running subcutanous suture. In
one group the skin wil be closed with a monoc
Sponsors
Catharina-ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: patient undergoing coronary artery bypass surgery with patent superficial saphenous vein
Exclusion criteria
Exclusion criteria: no
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| • Mean difference in treatment time • Mean difference in satisfaction score in patients • Mean difference in pain score • Incidence of adverse events e.g. wound infection • Mean difference satisfaction score of wound healing in experts (cardiothoracic surgeon and dermatologist) | — |
Secondary
| Measure | Time frame |
|---|---|
| • Mean difference in costs-efficiency • Mean difference in satisfaction score in attendants • Use of pain medication after surgery | — |
Countries
Netherlands
Outcome results
None listed