The Effects of Anesthesia Depth Monitoring on Postoperative Recovery and Cognitive Functions in the Geriatric Patient Population

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorAslıhan Güleç

About this trial

This study will be conducted on patients aged 65 and older scheduled for surgery due to lumbar or cervical disc herniation. General anesthesia is routinely used for these types of surgeries in the hospital. In patients receiving general anesthesia, anesthesia depth monitoring is performed.

As part of the study, a preoperative anesthesia evaluation will be conducted, which will include age, weight, height, comorbidities, regularly used medications, previous surgical or anesthesia experiences, nutritional habits, mental status, and daily activity levels.

On the day of surgery, upon arrival in the operating room, the following will be measured and recorded:

* Blood pressure using a non-invasive blood pressure monitor * Heart rate and rhythm via electrocardiogram (ECG) * Blood oxygen level with a pulse oximeter * Anesthesia depth using a forehead-applied sensor

All monitoring procedures are non-invasive and painless. Following the placement of these monitoring devices and initial measurements, anesthesia induction and surgery will commence. Throughout surgery, blood pressure, heart rate, and brain activity will be continuously recorded. After the surgical procedure, anesthesia emergence and mental status will be assessed. Preoperative evaluation data and intraoperative recordings will be used solely for research purposes, with patient identity information remaining confidential.

Eligibility criteria

Qualifiers

65 years and older

Elective spinal surgeries

ASA status I-III

Disqualifiers

Emergent surgeries

ASA status IV-V

Prediagnosed delirium and or dementia

Inability to give consent

Trial design

Treatments tested in this trial

  • Control Group: Standard Hemodynamic Monitoring
  • Processed Electroencephalogram (BIS Index)
  • Processed Electroencephalogram (DSA Mode)

Treatment groups

75 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Aslıhan Güleç

Lead sponsor

Gazi University

Sponsor institution