Efficacy and safety of oliceridine for treatment of moderate to severe pain after surgery with general anesthesia: a prospective, randomized, double-blinded, multicenter, positive-controlled clinical trial
10.3760/cma.j.cn131073.20231016.00203
- VernacularTitle:奥赛利定治疗全麻患者术后中重度疼痛的有效性和安全性：随机、盲法、阳性对照、多中心临床试验
- Author:
Gong CHEN
1
;
Wen OUYANG
;
Ruping DAI
;
Xiaoling HU
;
Huajing GUO
;
Haitao JIANG
;
Zhi-Ping WANG
;
Xiaoqing CHAI
;
Chunhui WANG
;
Zhongyuan XIA
;
Ailin LUO
;
Qiang WANG
;
Ruifeng ZENG
;
Yanjuan HUANG
;
Zhibin ZHAO
;
Saiying WANG
Author Information
1. 中南大学湘雅三医院麻醉科，长沙 410013
- Keywords:
Analgesics, opioid;
Pain, postoperative;
Pain management
- From:
Chinese Journal of Anesthesiology
2024;44(2):135-139
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To evaluate the efficacy and safety of oliceridine for treatment of moderate to severe pain after surgery with general anesthesia in patients.Methods:The patients with moderate to severe pain (numeric pain rating scale ≥4) after abdominal surgery with general anesthesia from 14 hospitals between July 6, 2021 and November 9, 2021 were included in this study. The patients were assigned to either experiment group or control group using a random number table method. Experiment group received oliceridine, while control group received morphine, and both groups were treated with a loading dose plus patient-controlled analgesia and supplemental doses for 24 h. The primary efficacy endpoint was the drug response rate within 24 h after giving the loading dose. Secondary efficacy endpoints included early (within 1 h after giving the loading dose) drug response rates and use of rescue medication. Safety endpoints encompassed the development of respiratory depression and other adverse reactions during treatment.Results:After randomization, both the full analysis set and safety analysis set comprised 180 cases, with 92 in experiment group and 88 in control group. The per-protocol set included 170 cases, with 86 in experiment group and 84 in control group. There were no statistically significant differences between the two groups in 24-h drug response rates, rescue analgesia rates, respiratory depression, and incidence of other adverse reactions ( P>0.05). The analysis of full analysis set showed that the experiment group had a higher drug response rate at 5-30 min after giving the loading dose compared to control group ( P<0.05). The per-protocol set analysis indicated that experiment group had a higher drug response rate at 5-15 min after giving the loading dose than control group ( P<0.05). Conclusions:When used for treatment of moderate to severe pain after surgery with general anesthesia in patients, oliceridine provides comparable analgesic efficacy to morphine, with a faster onset.
