Status:
NOT_YET_RECRUITING
Neuro-Mimic Indicators of Anesthesia Depth During General Anesthesia
Lead Sponsor:
Başakşehir Çam & Sakura City Hospital
Conditions:
General Anesthesia
Intraoperative Awareness
Eligibility:
All Genders
18-65 years
Brief Summary
This prospective observational study will evaluate neuro-mimic indicators of anesthesia depth, including eyelid reflex, eyeball movements, and pupil responses, in patients undergoing elective surgery ...
Detailed Description
Accurate assessment of anesthesia depth is essential to ensure patient safety and reduce the risk of intraoperative awareness. Current technological monitoring tools such as BIS do not always provide ...
Eligibility Criteria
Inclusion
- The study will include patients aged 18-65 who will undergo elective abdominal surgery (e.g., cholecystectomy/gastrectomy/colorectal surgery/prostatectomy/hysterectomy, etc.) under general anesthesia, with a planned duration of 1-3 hours.
- Patients whose eye area is left uncovered and who are in a position suitable for observation
- Patients who have signed the informed consent form
- Patients with an ASA score of I-III
Exclusion
- Patients undergoing surgical procedures in the head, neck, or face region (e.g., ENT, eye, jaw surgery, neurosurgery, thyroid/parathyroid)
- Patients whose eye area must be completely covered with a sterile drape
- Patients with an ASA score of IV or higher
- Individuals with neurological disorders and impaired pupil response, patients who have previously undergone eye trauma or surgery and cannot undergo pupil evaluation
- Patients who are unable to communicate and cannot provide informed consent
- Emergency surgeries (e.g., appendectomy/ileus/gastrointestinal perforation/cesarean section/gunshot wounds/stab wounds/multiple trauma/traffic accidents, etc.)
- Individuals who have previously been included in this study (to prevent repeated inclusion)
Key Trial Info
Start Date :
February 3 2026
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 28 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT07199049
Start Date
February 3 2026
End Date
July 28 2026
Last Update
January 6 2026
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