RecruitingNot ApplicableNCT06844279

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

Geriatrik Hasta Grubunda Anestezi Derinliği Monitörizasyonlarının Postoperatif Derlenme ve Bilişsel Fonksiyonlara Etkileri


Sponsor

Aslıhan Güleç

Enrollment

75 participants

Start Date

Jan 10, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 65 Years

Inclusion Criteria3

  • years and older
  • Elective spinal surgeries
  • ASA status I-III

Exclusion Criteria4

  • Emergent surgeries
  • ASA status IV-V
  • Prediagnosed delirium and or dementia
  • Inability to give consent

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERControl Group: Standard Hemodynamic Monitoring

Anesthesia depth monitoring based on hemodynamic values without additional processed EEG guidance.

DEVICEProcessed Electroencephalogram (BIS Index)

Anaesthesia depth monitoring according to numeric BIS index values.

DEVICEProcessed Electroencephalogram (DSA Mode)

Anaesthesia depth monitoring according to density spectral array functions


Locations(1)

Gazi University School of Medicine

Ankara, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06844279


Related Trials