Influence of Nociception Level Monitor (NOL) Guided Analgesic Delivery on Robot-assisted Colorectal Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of Southern Denmark

About this trial

Being relatively new, the NOL monitor may offer interesting observations in perioperative nociception levels and appropriate analgesic consumption in diverse surgeries, including robot-assisted surgery. These observations may supplement the current efforts towards further advantages in rapid restitution. Therefore, the investigators planned a trial where intra-operative analgesics were guided using an NOL monitor to study if intra-operative NOL guidance influences peri-operative analgesic consumption, postoperative length of stay and quality of recovery of patients subjected for robot-assisted surgery.

Eligibility criteria

Qualifiers

American Society of Anaesthesiologists score III-IV

Scheduled for elective major robot-assisted colorectal surgeries

Disqualifiers

Inability to give informed consent

planned spinal or epidural anaesthesia

all forms of regional anaesthesia, including wound infiltration

nonelective procedures

Trial design

Treatments tested in this trial

  • Nociception Level monitor (NOL)
  • Standard care

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators