50
Participants
Start Date
February 19, 2020
Primary Completion Date
March 14, 2022
Study Completion Date
June 14, 2022
Erector Spinae Catheter
Patients in the experimental group will receive the Erector Spinae Catheter with an initial bolus ob 20ml 0,5% levobupivacaine prior the surgery and will be administered local anesthetics for 48 hours post-operatively.
Intercostal block
Patients in the comparative group will receive standard treatment, i.e. the multi-level intercostal block with 20ml 0,5% levobupivacaine administered at the end of the surgery by the surgeon.
Ropivacaine 0.2% Injectable Solution
Patients in the experimental group will receive Ropivacaine 0,2% continous infusion of 5ml/h with boluses 15ml/4h by the Erector Spinae Catheter for 48 hours post-operatively.
Surgery Bitenc, Golnik
Surgery Bitenc
OTHER