NOL Guided Analgesia During Elective Laparoscopic Surgery Under General Anesthesia
ConditionIntraoperative Analgesia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorAttikon Hospital
About this trial
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
Qualifiers
Adult patients undergoing planned laparoscopic surgery under general anesthesia.
Disqualifiers
Emergency surgery.
Pregnancy.
Drug or alcohol abuse in the last 6 months.
Chronic opioid use or patients with chronic pain.
Trial design
Treatments tested in this trial
- Nociception level index (NOL™)
- Fentanyl
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov