EEG and ANI Guided Anesthesia and Quality of Recovery
Recruiting now · Not applicable
Conditions studied: Laparoscopic Gynecological Surgery
In brief
This study aims to assess whether electroencephalogram (EEG) and nociception level-guided anesthesia can improve quality of recovery after laparoscopic gynecological surgery compared with standard care. Patients will be randomly assigned to either EEG and Analgesia Nociception Index (ANI)-guided anesthesia group (EEG-and-ANI-Guided group) or usual care group (control group). Primary outcome is 15-item Quality of Recovery (QoR-15) score at postoperative day (POD) 1. Secondary outcomes included remifentanil consumption during anesthesia, occurrence of awareness with recall, incidence of undesirable intraoperative movement, emergence time, postoperative pain scores, quality of recovery score at POD 2, and length of hospital stay.
Key facts
- Study ID
- NCT05936671
- Run by
- Gangnam Severance Hospital
- People needed
- 126
- Starts
- 2023-07-13
- Expected to finish
- 2027-06-25
- Last updated by the study team
- 2026-07-23
Who can join
Age: 19 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Adult female patients who are scheduled to undergo laparoscopic gynecological surgery.
- Total laparoscopic hysterectomy with/without salpingo-oophorectomy
- Laparoscopic myomectomy
- Laparoscope-guided salpingo-oophorectomy
- Laparoscope-guided ovarian cystectomy
- Laparoscope-guided enucleation of ovarian cyst
You may not qualify if…
- Patients with nonregular sinus cardiac rhythm
- Patients with implanted pacemakers
- Patients on antimuscarinic agents, α2-adrenergic agonists, β1-adrenergic antagonists, antiarrhythmic agents
- pregnant or breastfeeding women
- Patients who are unable to communicate
Where it is running
- GangnamSeverance Hospital — Seoul, Seoul, South Korea (enrolling)
- Gangnam Severance Hospital — Seoul, Seoul, South Korea
Full record on ClinicalTrials.gov
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