Geneva, June 22 -- International Clinical Trials Registry received information related to the study (ChiCTR2600126674) titled 'Comparative Efficacy of Oliceridine and Sufentanil in Laparoscopic Postoperative Analgesia: Impact on Pain Relief and Hyperalgesia' on June 13.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Jilin Provincial People's Hospital
Condition:
Pain
Intervention:
Trial group (Oxycodine group):Induction: Oxycodine 0.04-0.1 mg/kg (maximum total dose 3 mg), half of induction dose given 10 minutes before incision, with intraoperative supplementation. Postoperative analgesia: Patient-controlled intravenous analgesia (PCIA), Oxycodine 0.2 mg/ml, total volume 100 ml, bolus dose 2 ml, continuous ...