Actively Recruiting
NOL Guided Analgesia During Elective Laparoscopic Surgery Under General Anesthesia
Led by Attikon Hospital · Updated on 2025-04-03
50
Participants Needed
1
Research Sites
178 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
NOL Guided Analgesia During Elective Laparoscopic Surgery Under General Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients undergoing planned laparoscopic surgery under general anesthesia.
You will not qualify if you...
- 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.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
2nd Department of Anesthesiology, Attikon University Hospital
Athens, Attica, Greece, 12462
Actively Recruiting
Research Team
P
PARASKEVI Prof MATSOTA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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