About this trial
The goal of this observational study is to learn about the analgesic efficacy and postoperative recovery of two locoregional anesthesia combinations in patients \> 18 years (ASA I-III), scheduled for unilateral TKA under spinal anesthesia with expected hospitalization \> 24 hours:
* ACB + sacral ESP block * ACB + iPACK block
The main question it aims to answer is: Does the ACB + sacral ESP block combination produce effective postoperative recovery and analgesic effect?
Participants already taking ACB + sacral ESP block as part of their regular peri-operative care for TKA will be followed in the postoperative period for 48 hours.
Eligibility criteria
Qualifiers
Adults >18 years
ASA I-III
scheduled for unilateral TKA with expected hospitalization > 24 hours
Disqualifiers
Refusal of consent
Local anesthetics allergies
contraindications to spinal or regional anesthesia
coagulation disorders
Trial design
Treatments tested in this trial
- Local Anesthetic Injection