Actively Recruiting
Influence of Nociception Level Monitor (NOL) Guided Analgesic Delivery on Robot-assisted Colorectal Surgery
Led by University of Southern Denmark · Updated on 2026-05-14
60
Participants Needed
1
Research Sites
191 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Influence of Nociception Level Monitor (NOL) Guided Analgesic Delivery on Robot-assisted Colorectal Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- American Society of Anaesthesiologists score III-IV
- Scheduled for elective major robot-assisted colorectal surgeries
You will not qualify if you...
- Inability to give informed consent
- Planned spinal or epidural anesthesia
- All forms of regional anesthesia, including wound infiltration
- Nonelective procedures
- Pregnancy or lactation
- Atrial fibrillation
AI-Screening
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Trial Site Locations
Total: 1 location
1
Anaesthesiology and Intensive Care Research Unit
Aabenraa, Denmark
Actively Recruiting
Research Team
T
Thomas Strøm
CONTACT
R
Rajesh Bhavsar
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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