Electroencephalographic Trajectories During Emergence From Inhalational and Total Intravenous Anesthesia
2 september 2026 uppdaterad av: Ruijin Hospital
General anesthesia emergence is a critical transition during which patients recover from an anesthetic-induced unconscious state to consciousness. This period is associated with various early postoperative complications, including emergence agitation, postoperative nausea and vomiting, delayed recovery, and impaired recovery quality in the Post-Anesthesia Care Unit (PACU). Although total intravenous anesthesia (TIVA) and inhalational anesthesia (IA) are widely used maintenance strategies, differences in their effects on cerebral recovery patterns during emergence remain incompletely understood.
Conventional assessments of emergence, such as time to eye opening, extubation time, and clinical sedation assessments, mainly reflect behavioral recovery and cannot directly characterize the dynamic process of cerebral functional recovery. Electroencephalography (EEG) provides continuous and non-invasive measurement of cortical activity and may enable objective characterization of anesthetic emergence.
Previous studies suggest that emergence from anesthesia involves dynamic transitions among distinct EEG states rather than a simple reversal of anesthetic induction, and specific EEG trajectories may be associated with abnormal emergence and PACU delirium. Therefore, this single-center prospective observational cohort study aims to continuously collect emergence-phase EEG data from patients receiving TIVA or IA without altering clinical anesthesia management. The study will compare EEG trajectory characteristics, spectral features, and aperiodic parameters between different anesthesia maintenance modalities and explore their associations with emergence quality and early postoperative complications.
This study may provide further insights into neurophysiological patterns of anesthetic emergence and support future optimization of emergence monitoring and perioperative management.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Studietyp
Observationell
Inskrivning (Beräknad)
140
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Qianzi Yang, MD, PhD
- Telefonnummer: +86 64370045
- E-post: yqz12471@rjh.com.cn
Studieorter
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Shanghai, Kina
- Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
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Kontakt:
- Qianzi Yang
- Telefonnummer: +86 64370045
- E-post: yqz12471@rjh.com.cn
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Ja
Testmetod
Icke-sannolikhetsprov
Studera befolkning
This study will enroll adult patients aged 18-60 years who are scheduled to undergo elective non-cardiac and non-neurosurgical surgery under general anesthesia.
Participants will receive routine clinical anesthesia management, and the choice of total intravenous anesthesia or inhalational anesthesia will be determined by the attending anesthesiologist according to clinical practice.
Beskrivning
Inclusion criteria
- Adults aged 18-60 years.
- Patients classified as American Society of Anesthesiologists (ASA) physical status I-III.
- Patients scheduled to undergo elective non-cardiac and non-neurosurgical surgery under general anesthesia.
- Expected duration of surgery ≥60 minutes.
- Expected intraoperative maintenance anesthesia with either total intravenous anesthesia (TIVA) or inhalational anesthesia .
- Patients who understand the study procedures and voluntarily provide written informed consent.
Exclusion Criteria
- History of central nervous system disorders, including epilepsy, Parkinson's disease, dementia, previous stroke with residual neurological deficits, or other clinically significant neurological diseases.
- Long-term use (≥4 weeks) of sedative-hypnotic drugs, antidepressants, antipsychotic medications, or other medications that may significantly affect central nervous system function.
- Pre-existing cognitive impairment or severe visual/hearing impairment preventing assessment of recovery of consciousness.
- Skin lesions, trauma, or other conditions affecting placement of frontal EEG electrodes.
- Emergency surgery, neurosurgery, cardiac surgery, planned deep sedation with postoperative intubation, or direct transfer to the intensive care unit after surgery.
- Severe intraoperative adverse events, including cardiac arrest, malignant hyperthermia, severe allergic reactions, major bleeding, or situations requiring substantial changes in the planned anesthesia maintenance strategy.
- Body mass index (BMI) ≥30 kg/m² or ≤18 kg/m².
- Refusal to participate or withdrawal of informed consent during the study.1. Adults aged 18-60 years, with no restriction on sex.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
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Inhalational anesthesia
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Ingen intervention: Observationskohort
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Total intravenous anesthesia
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Ingen intervention: Observationskohort
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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EEG trajectories during emergence from anesthesia
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation.
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Frontal EEG recordings will be analyzed to characterize spectral activity and its temporal evolution during emergence from general anesthesia.
Prespecified EEG parameters will include delta-band spectral power and alpha/spindle-band spectral power derived from power spectral density estimates.
These spectral features will be used to characterize EEG states and transitions during emergence, including state occupancy, transition timing, and transition sequences.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation.
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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EEG spectral power characteristics
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Frontal EEG recordings will be obtained during emergence from general anesthesia.
The EEG will be segmented into consecutive prespecified epochs, and spectral analysis will be performed for each segment.
Power spectral density will be calculated within the following frequency bands: delta, 0.5-4 Hz; theta, 4-8 Hz; alpha/spindle, 8-13 Hz; beta, 13-30 Hz; and gamma, 30-45 Hz.
Absolute power and relative power will be calculated for each frequency band.
Relative power will be defined as the power within each frequency band divided by the total spectral power across the prespecified analysis frequency range.
The alpha-to-delta power ratio, alpha peak frequency, and alpha peak power will also be calculated.
Gamma-band findings will be considered exploratory because of possible electromyographic contamination.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Aperiodic exponent of the EEG power spectrum
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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The aperiodic exponent will be estimated from frontal EEG power spectra using a prespecified spectral parameterization method that separates periodic spectral peaks from the aperiodic 1/f-like background.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Aperiodic offset of the EEG power spectrum
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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The aperiodic offset will be estimated from frontal EEG power spectra using a prespecified spectral parameterization method that separates periodic spectral peaks from the aperiodic 1/f-like background.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Auxiliary EEG and monitor-derived parameters during emergence
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Additional EEG-derived and monitor-generated parameters will be assessed during emergence from general anesthesia.
Spectral edge frequency 90% (SEF90) will be calculated as the frequency below which 90% of the total EEG spectral power within the prespecified analysis frequency range is contained.
In addition, the Ai Index and electromyographic (EMG) index generated by the EEG monitoring system will be recorded continuously during emergence.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Length of stay in the postanesthesia care unit
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Duration from admission to discharge from the postanesthesia care unit.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Aldrete score at PACU discharge
Tidsram: Before discharge from the postanesthesia care unit.
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Recovery status will be assessed using the Aldrete score at discharge from the postanesthesia care unit.
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Before discharge from the postanesthesia care unit.
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Richmond Agitation-Sedation Scale score at PACU discharge
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Level of agitation and sedation will be assessed using the Richmond Agitation-Sedation Scale (RASS) at PACU discharge.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Pain intensity measured using the Numeric Rating Scale at PACU discharge
Tidsram: From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Pain intensity will be assessed using the 0-10 Numeric Rating Scale (NRS) at PACU discharge, with higher scores indicating greater pain intensity.
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From discontinuation of the anesthetic maintenance drugs until 30 minutes after tracheal extubation
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Samarbetspartners och utredare
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Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
24 augusti 2026
Primärt slutförande (Beräknad)
31 mars 2027
Avslutad studie (Beräknad)
31 mars 2027
Studieregistreringsdatum
Först inskickad
24 augusti 2026
Först inskickad som uppfyllde QC-kriterierna
2 september 2026
Första postat (Faktisk)
8 september 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
8 september 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
2 september 2026
Senast verifierad
1 augusti 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- MR-31-26-069242
Läkemedels- och apparatinformation, studiedokument
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