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Study identifier: NCT07588165 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pain Assessment During Rapid Sequence Induction

Condition: Rapide Sequence Induction · Tracheal Intubation · Nociception  ·  Sponsor: Centre Hospitalier Princesse Grace

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Remy WIDEHEM  ·  +377 97 98 99 00  ·  remy.widehem@chpg.mc

Celine DUGOURD  ·  +377 97 98 84 29  ·  recherche.clinique@chpg.mc

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalier Princesse GraceMonaco, MonacoRecruiting

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Source record: clinicaltrials.gov/study/NCT07588165