Neuroinflammatory Biomarkers After General Anesthesia: A Comparison Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorUniversity of Health Sciences Balikesir Hospital Eduation and Research

About this trial

This prospective, observational study investigates the impact of repeated general anesthesia exposure on neuroinflammatory biomarkers and neurotrophic factors. The study will enroll 160 adult patients (aged 18-65 years) scheduled for elective cholecystectomy surgery, divided into two groups: patients with no previous general anesthesia exposure (n=80) and patients with at least one or more previous general anesthesia exposures (n=80).

Serum levels of Brain-Derived Neurotrophic Factor (BDNF), Interleukin-1 beta (IL-1β), and High Mobility Group Box 1 (HMGB1) will be measured using ELISA method at two time points: preoperatively (baseline) and 24 hours postoperatively. Cognitive function will also be assessed at both time points.

The primary objective is to evaluate whether multiple exposures to general anesthesia lead to significant differences in serum BDNF, IL-1β, and HMGB1 levels, reflecting changes in neurotrophic balance and neuroinflammatory response. This study aims to provide insights into the potential biochemical mechanisms underlying anesthesia-related cognitive changes and contribute original clinical data to the current literature on general anesthesia safety and neurobiological effects.

Eligibility criteria

Qualifiers

Age 18-65 years

Scheduled for elective cholecystectomy surgery

Either no previous general anesthesia exposure OR at least one or more previous general anesthesia exposures

Ability to provide informed consent

Disqualifiers

Chronic neurological diseases (Alzheimer's disease, Parkinson's disease, multiple sclerosis, etc.)

Psychiatric illness requiring medication

Metabolic syndrome (diabetes mellitus, hypertension, cardiac disease)

Chronic inflammatory diseases (rheumatoid arthritis, systemic lupus erythematosus, etc.)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

160 Participants
are grouped into 2 trial groups

Locations

This trial has no locations

Sponsors and collaborators