Overview

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