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Recruiting Observational

Evaluation of Intraoperative Awareness and Its Correlation With Processed EEG Biomarkers During Laparoscopic Surgery

NCT07831590 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-01
Last updated
2026-09-21

Condition(s) studied

Intraoperative AwarenessIntraoperative Responsiveness During General Anesthesia

Study summary

This prospective observational cohort study aims to evaluate intraoperative responsiveness and possible intraoperative awareness in adult patients undergoing elective laparoscopic abdominal surgery under general anesthesia and to investigate their relationship with processed electroencephalography (EEG) biomarkers.

Approximately 600 patients will be enrolled. Preoperative assessment will include the 15-item Quality of Recovery questionnaire (QoR-15), State-Trait Anxiety Inventory (STAI), Mini-Mental State Examination (MMSE), and Beck Anxiety Inventory (BAI).

Processed EEG monitoring will be performed using the Masimo SedLine system. The system will be applied before induction of general anesthesia and maintained throughout the anesthetic period until extubation. Patient State Index (PSI) values will be recorded at 5-minute intervals from the beginning of surgery until extubation.

The isolated forearm technique (IFT) will be performed five times during predefined stages of anesthesia and surgery. The fifth assessment will be performed at any stage of surgery when there is clinical or processed EEG evidence suggesting possible awakening, including a PSI value above 50 and/or accompanying hemodynamic changes such as tachycardia or hypertension.

Postoperative assessment will be performed at the 24th postoperative hour and at the second postoperative week. At 24 hours, QoR-15 and structured awareness questioning will be performed. At two weeks, QoR-15, Beck Anxiety Inventory, dream recall, and further assessment of possible intraoperative awareness will be performed.

The study will investigate the relationship between PSI changes, isolated forearm technique responses, and postoperative reports suggestive of intraoperative awareness.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Elective laparoscopic abdominal surgery planned * General anesthesia planned * Ability to communicate adequately * Adequate cognitive capacity to understand and respond to study procedures * ASA physical status I-III Exclusion Criteria: * Previous cerebrovascular disease * Psychiatric disorders * Cognitive dysfunction * ASA physical status \>III * High frailty * Body mass index \>30 kg/m² * Pregnancy * Age \<18 years

Primary outcome measure(s)

  • Association Between Positive Isolated Forearm Technique Responses and Patient State Index Changes — From the beginning of surgery until extubation
    The primary outcome is the association between positive responses obtained using the isolated forearm technique and changes in Patient State Index (PSI) values during general anesthesia. PSI values will be recorded at 5-minute intervals from the beginning of surgery until extubation. PSI changes occurring during or immediately surrounding positive IFT responses will be evaluated.

Trial sites (1)

FacilityCityRegionStatus
Duzce University Düzce Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07831590 on ClinicalTrials.gov ↗ ← All trials in Turkey