Geneva, April 20 -- International Clinical Trials Registry received information related to the study (NCT07525986) titled 'Anrikefon-based Patient-controlled Intravenous Analgesia Following Laparoscopic Surgery' on April 6.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
Primary Sponsor: Peking University First Hospital
Condition:
Anrikefon
Patient-controlled Intravenous Analgesia
Laparoscopic Surgery
Visceral Pain, Postoperative
Intervention:
Drug: High-dose anrikefon
Drug: Medium-dose anrikefon
Drug: Low-dose anrikefon
Recruitment Status: Not recruiting
Phase:...