Safety and efficacy of remimazolam besylate in patients undergoing colonoscopy: A multicentre, single-blind, randomized, controlled, phase Ⅲ trial
Study objective: The objective of the study was to evaluate the safety and efficacy of remimazolam besylate versus propofol injection in patients undergoing colonoscopy.Design: A multicenter, randomized, non-inferiority, single-blind, parallel-controlled clinical trial.Setting: Operating room.Patien...
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Frontiers Media S.A.,
2022-10-01T00:00:00Z.
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001 | doaj_8f79f641a58f45ce8d97caa2875c4502 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Ximei Wang |e author |
700 | 1 | 0 | |a Xiaolei Hu |e author |
700 | 1 | 0 | |a Nianyue Bai |e author |
700 | 1 | 0 | |a Lie Li |e author |
700 | 1 | 0 | |a Lie Li |e author |
700 | 1 | 0 | |a Min Zhang |e author |
700 | 1 | 0 | |a Zhigang Cheng |e author |
700 | 1 | 0 | |a Qulian Guo |e author |
245 | 0 | 0 | |a Safety and efficacy of remimazolam besylate in patients undergoing colonoscopy: A multicentre, single-blind, randomized, controlled, phase Ⅲ trial |
260 | |b Frontiers Media S.A., |c 2022-10-01T00:00:00Z. | ||
500 | |a 1663-9812 | ||
500 | |a 10.3389/fphar.2022.900723 | ||
520 | |a Study objective: The objective of the study was to evaluate the safety and efficacy of remimazolam besylate versus propofol injection in patients undergoing colonoscopy.Design: A multicenter, randomized, non-inferiority, single-blind, parallel-controlled clinical trial.Setting: Operating room.Patients: Patients aged 18-65 years (American Society of Anesthesiologists [ASA] classification I-III) undergoing a diagnostic or therapeutic colonoscopy.Interventions: Patients were administered intravenous injection of remimazolam besylate or propofol (active comparator) for sedation.Measurements: Modified Observer's Assessment of Alertness/Sedation [MOAA/S] scores of the included patients were assessed before dosing, 1, 1.5, 2, 2.5, and 3 min after the start of dosing, and then every 1 min until the MOAA/S score reached 5 on three consecutive occasions.Main Results: A total of 360 patients received remimazolam and 120 patients received propofol. The incidence of adverse events (67.8% vs. 84.2%, p = 0.001) was significantly lower in patients administered remimazolam compared to propofol. There was no significant difference in sedation success rates (full analysis set [FAS]: 98.9% vs. 99.2%; remimazolam vs. propofol). Remimazolam had a significantly longer onset of action, but the difference was not considered clinically significant (1.45 min vs. 1.24 min, remimazolam vs. propofol). Propofol achieved a deeper level of sedation (mean MOAA/S score 0.5 vs. 0.2; remimazolam vs. propofol). Mean time to discharge after the end of the last administration of study drug (20.3 vs. 21.8 min, p = 0.020) and incidence of injection pain was significantly lower in patients administered remimazolam (2.3% vs. 35.3%, p < 0.0001). Incidence of oxygen desaturation was significantly higher in patients administered propofol compared to patients administered remimazolam (6.7% vs. 1.1%, p = 0.001). Similarly, incidence of hypotension was more frequent in patients administered propofol compared to patients administered remimazolam (29.2% vs. 10.6%, p < 0.0001).Conclusion: Remimazolam besylate had a better safety and tolerability profile and similar sedative efficacy to propofol in patients undergoing a diagnostic or therapeutic colonoscopy in China, suggesting that remimazolam besylate has potential as a sedative agent for colonoscopy. | ||
546 | |a EN | ||
690 | |a remimazolam besylate | ||
690 | |a propofol | ||
690 | |a sedation | ||
690 | |a adverse | ||
690 | |a events | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Frontiers in Pharmacology, Vol 13 (2022) | |
787 | 0 | |n https://www.frontiersin.org/articles/10.3389/fphar.2022.900723/full | |
787 | 0 | |n https://doaj.org/toc/1663-9812 | |
856 | 4 | 1 | |u https://doaj.org/article/8f79f641a58f45ce8d97caa2875c4502 |z Connect to this object online. |