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NCT06104059
NOL Guided Analgesia During Elective Laparoscopic Surgery Under General Anesthesia
Conditions: Intraoperative Analgesia
Sex: All
Ages: 18 Years – 70 Years
Healthy volunteers: No
Phase: NA
Enrollment: 50
Sponsor: Attikon Hospital
Location: 2nd Department of Anesthesiology, Attikon University Hospital Athens Attica
Summary
The aim of this study is to investigate the hypothesis that the intraoperative use of the nociception level index NOL can reduce opioid consumption in adult patients undergoing elective laparoscopic surgeries under general anesthesia, as well as to explore its effect on post-operative pain and patient recovery.
Eligibility Criteria
Inclusion Criteria:
* Adult patients undergoing planned laparoscopic surgery under general anesthesia.
Exclusion Criteria:
* Emergency surgery.
* Pregnancy.
* Drug or alcohol abuse in the last 6 months.
* Chronic opioid use or patients with chronic pain.
* Serious comorbidity \[cardiac disease (atrial fibrillation, ventricular arrhythmias), liver or kidney disease\]
* Obesity (BMI \>35).
* Permanently implanted pacemaker.
* Patients with CNS disease.
* Allergy to any of the study drugs.
* Patients receiving anticholinergics agonists, α2-adrenergic agonists, β1-adrenergic antagonists, antiarrhythmic drugs.
Source: ClinicalTrials.gov (NCT06104059). StuddyBuddy aggregates publicly available trial information.
