Abstract:Methods This study is a double-blinded, randomized, controlled, prospective study, submitted to clinicaltrials.gov (NCT04879004). 30 patients scheduled for OC and LC were randomized into 4 equal groups. If the patient was randomized in Group R L or R O , Ropivacaine 0.375% (20 ml) was infused at each side 30 minutes before induction of GA and 0.2% (20 ml) 12, 24, 36 and 48 hours after surgery. If the patient was randomized in Group C L or C O , N/S 0.9% (20 ml) was infused in the same manner. We recorded QoR s… Show more
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