About this trial
This study will quantify the nociception using Analgesia Nociception Index (ANI) during general anesthesia and analyze the differences in EEG depending on the degree of nociception. Additionally, the investigators will quantify the nociception during recovery and analyze the differences in EEG depending on the degree of nociception.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Patients with arrhythmia
Patients with pacemaker implantation
Patients who have received a heart transplant
Patients taking medications that may affect ANI (antimuscarinics, alpha-agonist, beta blockers, etc.)
Trial population
Patients undergoing laparoscopic surgery
Trial design
Cohort
Prospective
Treatments tested in this trial
There is no Intervention name to describe.
Other interventionThere is no Intervention name to describe.
Treatment groups
Trial outcomes
Primary outcomes
Correlation between changes in ANI and EEG band power in response to surgical stimulation.
Correlation between changes in ANI and EEG band power in response to surgical stimulation
Secondary outcomes
Correlation between changes in ANI and EEG band power in response to tracheal intubation
Correlation between changes in ANI and EEG band power in response to tracheal intubation
Correlation between changes in ANI and EEG connectivity in response to surgical stimulation
Correlation between changes in ANI and EEG connectivity in response to surgical stimulation
Correlation between changes in ANI and EEG connectivity in response to tracheal intubation
Correlation between changes in ANI and EEG connectivity in response to tracheal intubation
Correlation between changes in ANI, EEG band power and NRS in response to analgesic administration
Correlation between changes in ANI, EEG band power and NRS in response to analgesic administration
Sponsors and contacts
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