Trial reportBMC anesthesiology2025
Effect of continuous cuff pressure regulator on postoperative sore throat in patients undergoing laparoscopic cholecystectomy with H-LMA: a randomized controlled trial.
Trial report in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe aim of this study was to investigate the effect of continuous regulation of laryngeal mask cuff pressure on postoperative sore throat (POST) after laparoscopic cholecystectomy.
methodsPatients underwent laparoscopic cholecystectomy were randomly divided into group E or group C in a 1:1 ratio. Laryngeal mask was inserted after successful induction of general anaesthesia. The product of laryngeal mask used in this study was Hope laryngeal mask airway (H-LMA). Group E: the continuous cuff pressure regulator was used to continuously control the cuff pressure of the laryngeal mask at 40 cmH
resultsA total of 100 adult patients completed the study. The incidence of POST 30 min and within 24 h of extubation was lower in group E than in group C (12% vs. 36%; P = 0.009) (10% vs. 32%; P = 0.013). The severity of POST 30 min and within 24 h after extubation was also lower in group E than in group C (all P<0.05). The incidence of dysphagia 30 min and within 24 h after extubation was lower in group E than in group C (all P<0.05).
conclusionsIn conclusion, the incidence of POST can be reduced by continuously controlling the laryngeal mask cuff pressure at 40 cmH
trial registrationChinese Clinical Trial Registry identifier: ChiCTR2400093522. (Principal investigator: Gongchen Duan; registration date: 6 December 2024).
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