Using NOL to guide pain management during laparoscopic surgery
Official title: Ιntraoperative Administration of Opioids Guided by the Nociception Level Index NOL in Elective Laparoscopic Surgeries Under General Anesthesia: Effect on Opioid Consumption, Post-operative Pain and Patient Recovery
Run by Attikon Hospital · NCT06104059 · Data updated 2026-11-12
This study tests if using a special pain measurement tool can help adults having laparoscopic surgery use fewer opioids and recover better after their procedure.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Attikon Hospital Academic / other |
| Locations | 1 site (Athens, Attica) |
| Status | Recruiting |
| Started | April 20, 2023 |
| Main results expected | September 20, 2027 |
| Study ends | September 20, 2028 |
| Registry record updated | October 30, 2026 |
| Trial ID | NCT06104059 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adult patients over 18 years old scheduled for elective laparoscopic surgery under general anesthesia.
✕Probably not a fit
Patients who may not benefit include those undergoing emergency surgeries, pregnant individuals, or those with chronic pain or serious comorbidities.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates whether the nociception level index (NOL) can effectively reduce opioid consumption in adult patients undergoing elective laparoscopic surgeries under general anesthesia. Patients will be randomly assigned to either an intervention group, where NOL is used to guide analgesia, or a control group receiving standard anesthetic care. The study aims to assess the impact of NOL on postoperative pain and recovery outcomes. Standard monitoring and anesthesia protocols will be followed for all participants.
Why it matters
Potential benefit: If successful, this approach could lead to reduced opioid use and improved recovery for patients undergoing laparoscopic surgery.
How similar studies have gone: Other studies have shown promise in using nociception monitoring to guide analgesia, suggesting potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion 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.
Where it's running
-
2nd Department of Anesthesiology, Attikon University Hospital
Athens, Attica, Greece Recruiting
Study contacts
- Study coordinator: PARASKEVI Prof MATSOTA
- Email: matsota@yahoo.gr
- Phone: 6945544563
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.