Comparison of Postoperative Nociception Between NOL-guided and Standard Intraoperative Analgesia Based on Fentanyl (NOLFentanyl)
Pain, Postoperative, Opioid Use, Nociceptive Pain
About this trial
This is an interventional prevention trial for Pain, Postoperative focused on measuring pain, Postoperative Pain, fentanyl, Nociceptive monitoring index
Eligibility Criteria
Inclusion Criteria:
- ASA I-II
- Elective abdominal surgery without a neuraxial block.
- Over 2 horas.
- Body Mass Index 18 - 30 kg/m2
Exclusion Criteria:
- Cardiac surgery
- Cardiopathy
- Arrhythmia or use of pacemakers.
- Chronic Kidney disease (Plasma Crea >1 mg/dL).
- Allergic to drugs of this study.
- Opioids or Non-inflammatory drugs over 5 days for two weeks before surgery.
- Neuropathies and dysautonomias.
- Beta-blockers and other drugs that act at the level of the sympathetic system the month prior to surgery.
- Chemotherapy.
Sites / Locations
- Victor Contreras
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
fentanyl NOL guided
fentanyl standard analgesia
A bolus of 2 mcg/kg IV Fentanyl will be given at the induction of the anesthesia. A bolus of 0,5 - 1 mcg/kg IV Fentanyl will be given at the time of incision and during surgery following a predeterminate NOL index + heart rate + mean arterial blood pressure variations.
A bolus of 2 mcg/kg IV Fentanyl will be given at the induction of the anesthesia. A bolus of 0,5 - 1 mcg/kg IV Fentanyl will be given at the time of incision and during surgery following the heart rate and mean arterial blood pressure variations.