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Pain Assessment During Rapid Sequence Induction

Recruitingn/aAges 18 Years - anyAllCentre Hospitalier Princesse Grace
NCT07588165 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Rapid sequence induction (RSI) is a standard anesthesia technique used in patients at risk of aspiration. Although tracheal intubation following RSI is a frequent and painful procedure, no study has yet evaluated nociception using the Analgesia Nociception Index (ANI) during this procedure. This monocentric prospective observational study aims to describe the impact of RSI on pain measured by ANI, and to explore early complications (desaturation, hypotension, regurgitation) and factors associated with pain and complications. 150 patients undergoing RSI in the visceral surgery operating room at CHPG Monaco will be analyzed.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Age \>= 18 years * Patient requiring tracheal intubation after rapid sequence induction in the visceral surgery operating room * Pain monitoring by Analgesia Nociception Index (ANI) as part of general anesthesia Exclusion Criteria: * Patient with atrial fibrillation at the time of intubation following rapid sequence induction * Patient on long-term beta-blocker therapy
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What it tests

  • No Intervention: Observational Cohort
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Where

1 site
Centre Hospitalier Princesse Grace
Monaco, Monaco
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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