Automatic Remifentanil Administration Guided by ANI During Propofol Anesthesia

• Status: Recruiting
• Trial end date: 2021-06-01
• Target enrollment: 0
• Participant gender: All

Summary

Prospective Randomized Monocentric Clinical Trial during propofol anesthesia. The aim of the study is to test whether the use of a medical device designed to automatically administer remifentanil during surgery based on expert rules and continuous reading of heart rate, blood pressure and the Analgesia Nociception Index results in lower overall remifentanil administration versus standard practice.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University Hospital, Lille
• Treatments: Anesthetics; Propofol; Remifentanil

Criteria

Inclusion Criteria:

• ASA 1, 2 or 3 adult patients scheduled to undergo burn wound surgery at the Burn Center of the University Hospital of Lille

Exclusion Criteria:

• BMI outside [17 - 35 kg/m2]

• pregnancy or breast feeding women

• non sinus cardiac rhythm

• documented dysautonomia

• complicated diabetes mellitus

• known allergy to a drug used in the clinical trial