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March 1, 2026SHILAP Revista de lepidopterología0 citationsOpen Access

Effect of deep analgosedation vs. intubated general anesthesia on perioperative sedation-related adverse events in older adults undergoing ERCP: protocol for a randomized controlled trial

XLXiaocui LvYXYu XuJSJianliang Sun

Key Points

  • This trial aims to determine the optimal analgosedation strategy for older adults undergoing ERCP by comparing NPA-assisted DAS and endotracheal intubation GA.
  • Patients scheduled for ERCP randomly assigned to NPA-assisted DAS or endotracheal intubation GA.
  • Randomization stratified by study center and hypertension status using permuted blocks.
  • Primary outcome: composite of sedation-related adverse events including hypoxemia and hypotension.
  • Secondary outcomes: various patient recovery metrics and satisfaction.
  • Detailed findings will assess differences in sedation-related adverse events between both groups.
  • Patient outcomes on recovery time, satisfaction, and overall safety will be compared.

Abstract

Background Deep analgosedation (DAS) and general anesthesia (GA) are currently the predominant anesthetic approaches for endoscopic retrograde cholangiopancreatography (ERCP). In contrast to DAS, GA typically requires endotracheal intubation for airway management. To determine the optimal analgosedation strategy, this study is designed to compare the effect of nasopharyngeal airway-assisted DAS (NPA-assisted DAS) vs. endotracheal intubation GA on perioperative sedation-related adverse events (SRAEs) in elderly ERCP patients. Methods Patients scheduled for ERCP will be randomly assigned in a 1:1 ratio to NPA-assisted DAS or endotracheal intubation GA. Randomization will be stratified by study center and hypertension status, using permuted blocks of sizes 2 and 4. The major exclusion criterion is severe cardiopulmonary disease. The primary outcome is a composite of SRAEs, including hypoxemia, hypotension, hypertension, laryngospasm, or bronchospasm. Secondary outcomes include escalation of respiratory support, tachycardia, bradycardia, reflux, recovery time, postoperative recovery quality (QoR-15), postoperative nausea and vomiting (PONV), cognitive function, perioperative respiratory failure or acute respiratory distress syndrome (ARDS), patient and endoscopist satisfaction, and length of hospital stay. All analyses will follow a modified intention-to-treat approach. Ethics and dissemination Ethics approval was obtained from the Ethics Committee of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine (2025-0780). Written informed consent will be obtained from all participants prior to enrollment. The findings of this trial will be disseminated through publication in a peer-reviewed journal. Trial registration number Clinical Trial Registry (NCT07017283).

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Cite This Study

Lv et al. (2026) studied this question.

synapsesocial.com/papers/69a3d79dec16d51705d2dd47https://doi.org/10.3389/fmed.2026.1764649
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