Pain monitoring with ANI during rapid sequence induction

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center prospective observational study in Monaco that describes how RSI affects nociception as measured by ANI in adults. Researchers will monitor ANI alongside standard anesthesia care to explore pain levels and early complications such as desaturation, hypotension, and regurgitation. Induction drugs are chosen by the treating anesthesiologist, and ANI monitoring uses non-invasive electrodes during the procedure.

Why it matters

Who can join: the full rules

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

Where it's running

• Centre Hospitalier Princesse Grace
  Monaco, Monaco Recruiting

Study contacts

• Principal investigator: Remy WIDEHEM, MD — Centre Hospitalier Princesse Grace
• Study coordinator: Remy WIDEHEM
• Email: remy.widehem@chpg.mc
• Phone: +377 97 98 99 00

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.