About this trial
The goal of this clinical trial is to learn if patients remaining different positions for 30min after receiving ultrasound-guided erector spinae plane block influenced the postoperative analgesia. The main questions it aims to answer are:
Does patients maintain prone position or lateral position for 30 min after ESPB provided superior analgesic effect than in the supine position? Is ESPB not inferior to PVB considering postoperative opioid consumption ? Researchers will compare the opioid consumption 24h postoperatively among the patients remaining supine, lateral, prone position after ESPB and PVB to see if patients maintaining lateral or prone position provided excellent postoperative analgesia.
Participants will:
Maintaining supine lateral or prone position for 30 min following ESPB or receiving PVB.
Receiving postoperative NRS and QoR assessment
Eligibility criteria
Qualifiers
None
Disqualifiers
Allergy to the study drug or allergy to local anaesthetics;
History of opioid abuse;
Previous nerve block puncture with puncture site infection;
Peripheral neuropathy;
Trial design
Treatments tested in this trial
- position