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RecruitingNCT05936671Updated Jul 23, 2026

EEG and ANI Guided Anesthesia and Quality of Recovery

An interventional study of EEG-and-ANI-guided anesthesia and standard anesthesia in Laparoscopic Gynecological Surgery, sponsored by Gangnam Severance Hospital. Recruiting at 2 sites in South Korea. Open to female participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-07-23.

Sponsored by Gangnam Severance Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2023; still recruiting 3 years 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
126
Allocation
Randomized
Ages
19 Years and older
Sex
Female
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Study summary

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.

Read the detailed description

Adult women scheduled to undergo laparoscopic gynecologic surgery will be screened for eligibility. Patients will be randomly allocate to either the EEG-and-ANI-guided group or usual care group.

In the guided group, sevoflurane concentration will be titrated according to EEG monitoring. Intraoperative infusion of remifentanil will be titrated by ANI monitoring.

In the usual care group, EEG and ANI sensor will be attached to patients, but EEG and ANI monitor will be blinded to the attending anesthesiologists. The anesthesiologists will provide a standard care of our institution for anesthetic and analgesic titration. In brief, hemodynamic variables and clinical situations will be used to titrate the anesthetic depth and analgesic dose.

Blinded investigator will assess quality of recovery questionnaire-15 at postoperative day 1 and 2.

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Conditions studied

  • Laparoscopic Gynecological Surgery
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In context

Lead sponsor

Gangnam Severance Hospital is the lead sponsor of 146 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Adult female patients who are scheduled to undergo laparoscopic gynecological surgery.

  1. Total laparoscopic hysterectomy with/without salpingo-oophorectomy
  2. Laparoscopic myomectomy
  3. Laparoscope-guided salpingo-oophorectomy
  4. Laparoscope-guided ovarian cystectomy
  5. Laparoscope-guided enucleation of ovarian cyst

Exclusion criteria

Exclusion Criteria:

  1. Patients with nonregular sinus cardiac rhythm
  2. Patients with implanted pacemakers
  3. Patients on antimuscarinic agents, α2-adrenergic agonists, β1-adrenergic antagonists, antiarrhythmic agents
  4. pregnant or breastfeeding women
  5. Patients who are unable to communicate
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
126 participants (estimated)

Study arms

  • Experimental
    EEG-and-ANI-guided group

    During anesthetic maintenance, sevoflurane concentration will be titrated according to EEG monitoring. Sevoflurane concentration will be titrated to maintain intraoperative Patient state index (PSi) ≥ 35 and to avoid burst suppression. Intraoperative target-controlled infusion of remifentanil will be titrated to maintain intraoperative ANI between 50 and 70.

    Procedure: EEG-and-ANI-guided anesthesia · Drug: Sevoflurane and remifentanil · Device: EEG and ANI

  • Active comparator
    Usual care group

    During anesthetic maintenance, the attending anesthesiologists will provide a routine standard care for anesthetic and analgesic titration. In brief, hemodynamic variables and clinical situations will be used to titrate the sevoflurane concentration and remifentanil infusion rates.

    Procedure: standard anesthesia · Drug: Sevoflurane and remifentanil

Interventions

  • ProcedureEEG-and-ANI-guided anesthesia

    During anesthetic maintenance, sevoflurane concentration will be titrated according to EEG monitoring. Sevoflurane concentration will be titrated to maintain intraoperative Patient state index (PSi) ≥ 35 and to avoid burst suppression. Intraoperative target-controlled infusion of remifentanil will be titrated to maintain intraoperative ANI between 50 and 70.

  • Procedurestandard anesthesia

    During anesthetic maintenance, the attending anesthesiologists will provide a routine standard care for anesthetic and analgesic titration. In brief, hemodynamic variables and clinical situations will be used to titrate the sevoflurane concentration and remifentanil infusion rates.

  • DrugSevoflurane and remifentanil

    Drug pages: Sevoflurane · Remifentanil

    For anesthetic maintenance, balanced anesthesia with sevoflurane inhalation and target controlled infusion of remifentanil will be performed.

  • DeviceEEG and ANI

    EEG monitoring using SEDline (Masimo, Irvine, California, USA) and Analgesia Nociception Index (ANI; MetroDoloris Medical Systems, Lille, France) monitoring will be performed.

06

What researchers measure

Primary outcomes

  1. 15-item Quality of Recovery (QoR-15) at postoperative day (POD) #1

    The Korean version of 15-item Quality of Recovery (QoR-15) score. Each item uses an 11-point numeric rating scale. The sum of the scores of the 15 items ranges from 0 to 150, with a high score indicating good quality of recovery.

    Time frame: 24 hours after the end of surgery

Secondary outcomes

  1. Remifentanil consumption during anesthesia

    Total remifentanil consumption during anesthesia

    Time frame: During surgery, from the anesthetic induction to emergence of anesthesia

  2. Occurrence of awareness with recall

    Occurrence of awareness with recall during surgery, which will be asked at postoperative day #1.

    Time frame: During the operation.

  3. Incidence of undesirable intraoperative movement

    Incidence of undesirable intraoperative movement during surgery

    Time frame: During the operation.

  4. Intraoperative end-tidal sevoflurane minimum alveolar concentration (MAC)

    Intraoperative end-tidal sevoflurane minimum alveolar concentration (MAC)

    Time frame: During the operation

  5. Intraoperative time ANI <50 [%]

    Intraoperative time of ANI value \<50 / total duration of surgery (%)

    Time frame: During the operation.

  6. Intraoperative mean PSi

    Intraoperative mean Patient state index (a processed EEG parameter related to a patient's current level of sedation/anesthesia along a scale of 0 to 100, where 100 represents being fully awake)

    Time frame: During the operation.

  7. Intraoperative mean ANI

    Intraoperative mean Analgesia Nociception Index (expressed on a non-unit scale of 0-100; 100 indicates maximal relative parasympathetic tone)

    Time frame: During the operation.

  8. Intraoperative EEG burst suppression

    Intraoperative occurrence of burst suppression on electroencephalogram

    Time frame: During the operation

  9. burst suppression ratio

    Intraoperative burst suppression ratio on electroencephalogram

    Time frame: During the operation

  10. burst suppression duration

    duration of burst suppression on electroencephalogram

    Time frame: During the operation

  11. Emergence time

    time between reversal of neuromuscular block and extubation

    Time frame: From time of administration of reversal agents of neuromuscular block until time of extubation, assessed up to 2 hours

  12. Intraoperative hypotension

    Incidence of hypotension during surgery

    Time frame: During the operation

  13. Intraoperative phenylephrine consumption

    total dose of phenylephrine consumption during surgery

    Time frame: During the operation.

  14. Pain numeric rating scale (NRS)

    NRS (0 to 10, with 0 being "no pain" and 10 being "the worst pain imaginable ") pain scores during post-anesthesia care unit (PACU) stay, at postoperative 24, 48 hours

    Time frame: scores during post-anesthesia care unit (PACU) stay, at postoperative 24, 48 hours

  15. The incidence of post-operative nausea and vomiting

    The incidence of post-operative nausea and vomiting

    Time frame: during the post-anesthesia care unit (PACU) stay, at postoperative day 1, 2

  16. Patient satisfaction with anesthetic management

    Patient satisfaction with overall anesthetic management in 11-point scale (0-10), The higher the score, the higher the patient's satisfaction.

    Time frame: At post-operative 24 hours

  17. Quality of Recovery Questionnaire (15-item Quality of Recovery) at postoperative day #2

    Each item uses an 11-point numeric rating scale. The sum of the scores of the 15 items ranges from 0 to 150, with a high score indicating good quality of recovery.

    Time frame: At post-operative 48 hours

  18. shivering, airway obstruction, respiratory depression, sedation in PACU

    Incidence of shivering, airway obstruction, respiratory depression, sedation

    Time frame: from time of the post-anesthesia care unit (PACU) admission to time of discharge from PACU, assessed up to 2 hours

  19. Hospital length of stay

    Hospital length of stay

    Time frame: From date of hospital admission until the date of hospital discharge, assessed up to 100 weeks

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Study locations

1 of 2 sites recruiting
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References and documents

Publications

  • Punjasawadwong Y, Phongchiewboon A, Bunchungmongkol N. Bispectral index for improving anaesthetic delivery and postoperative recovery. Cochrane Database Syst Rev. 2014 Jun 17;2014(6):CD003843. doi: 10.1002/14651858.CD003843.pub3. PubMed 24937564 ↗
  • Upton HD, Ludbrook GL, Wing A, Sleigh JW. Intraoperative "Analgesia Nociception Index"-Guided Fentanyl Administration During Sevoflurane Anesthesia in Lumbar Discectomy and Laminectomy: A Randomized Clinical Trial. Anesth Analg. 2017 Jul;125(1):81-90. doi: 10.1213/ANE.0000000000001984. PubMed 28598927 ↗
  • Espitalier F, Idrissi M, Fortier A, Belanger ME, Carrara L, Dakhlallah S, Rivard C, Brulotte V, Zaphiratos V, Loubert C, Godin N, Fortier LP, Verdonck O, Richebe P. "Impact of Nociception Level (NOL) index intraoperative guidance of fentanyl administration on opioid consumption, postoperative pain scores and recovery in patients undergoing gynecological laparoscopic surgery. A randomized controlled trial". J Clin Anesth. 2021 Dec;75:110497. doi: 10.1016/j.jclinane.2021.110497. Epub 2021 Sep 28. PubMed 34597955 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05936671
Responsible party
Dong Woo Han (Professor, Gangnam Severance Hospital) — Principal investigator
First posted
Jul 10, 2023
Start date
Jul 13, 2023
Primary completion
Jun 19, 2027 (estimated)
Completion
Jun 25, 2027 (estimated)
Last update
Jul 23, 2026

Study contacts

Sun-Kyung Park, MD,PhD
Contact
mayskpark@gmail.com
821024505924
Dong Woo Han, MD,PhD
principal investigator · Gangnam Severance Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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