2,000
Participants
Start Date
February 7, 2023
Primary Completion Date
November 30, 2026
Study Completion Date
December 30, 2026
Esmolol
The treatment group was given Esmolol 0.5mg/kg load and 10μg /kg/min continuous pump
Placebo Comparator: Placebo Comparator:normal saline(0.9%)
The control group received the same volume of 0.9% normal saline, which was continuously pumped until the end of the operation before extubation.Patient-controlled analgesia pump (sufentanil 2 μg/kg, 2 mL/h, for 48h) was used as the postoperative analgesia regimen in the two groups. If the VAS score was \>3, analgesic adjuvant drugs were given intravenously and recorded. If repeated treatment is ineffective, the study will be excluded.
RECRUITING
Qianfoshan Hospital, The First Hospital affiliated of Shandong First Medical University, Jinan
Yongtao Sun
OTHER