Pain Assessment During Rapid Sequence Induction
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Princesse Grace
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Patient with atrial fibrillation at the time of intubation following rapid sequence induction
Patient on long-term beta-blocker therapy
Trial design
Treatments tested in this trial
- No Intervention: Observational Cohort
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov