126
Participants
Start Date
May 31, 2021
Primary Completion Date
September 30, 2025
Study Completion Date
December 31, 2025
Arm A : intraoperative ANI monitoring of nociception
For the experimental group (arm A), the sufentanil doses are adjusted to maintain an ANI between 50 and 70. Morphine doses are adjusted from 0.05 to 0.05 µg / ml. Intraoperative data will be collected for ANI, TIVA and hemodynamics.
Arm B : no specific monitoring of nociception
For the control group (arm B), adjustments to the opioid doses are made in relation to the hemodynamic reactions of the patient and the operating times. Intraoperative data will be collected for TIVA and hemodynamics.
RECRUITING
Institut Bergonié, Bordeaux
Lead Sponsor
Institut Bergonié
OTHER