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Pain Assessment During Rapid Sequence Induction

NCT07588165 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2026-05-27

No results posted yet for this study

Summary

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.

Conditions

  • Rapide Sequence Induction
  • Tracheal Intubation
  • Nociception
  • General Anesthesia

Interventions

OTHER

No Intervention: Observational Cohort

Standard rapid sequence induction according to SFAR guidelines, with additional non-invasive ANI monitoring via cutaneous pectoral electrodes. No intervention beyond routine care; induction drug choice (hypnotic, opioid, neuromuscular blocker) at the discretion of the anesthesiologist.

Sponsors & Collaborators

  • Centre Hospitalier Princesse Grace

    lead OTHER

Principal Investigators

  • Remy WIDEHEM, MD · Centre Hospitalier Princesse Grace

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-21
Primary Completion
2028-05-31
Completion
2028-05-31

Countries

  • Monaco

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07588165 on ClinicalTrials.gov