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Recruiting Observational

Perioperative GFAP and Neurological Complications After Carotid Endarterectomy

NCT07843979 · tracked via the Priya Life Science Turkey tracker
Sponsor
Filiz Ata
Phase
Observational
Started
2025-12-15
Last updated
2026-09-28

Condition(s) studied

Carotid Stenosis

Investigational drug(s) / intervention(s)

Serum GFAP Measurement

Serum GFAP Measurement: Serum glial fibrillary acidic protein (GFAP) is measured before carotid endarterectomy and 24 hours after surgery. The measurements are collected for observational analysis and do not determine the participant's clinical care.

Study summary

This prospective, single-center observational study will evaluate whether blood levels of glial fibrillary acidic protein (GFAP), a protein associated with injury to supporting cells in the brain, are related to neurological complications after carotid endarterectomy. Adults aged 35 to 90 years undergoing elective isolated carotid endarterectomy will be enrolled. Serum GFAP will be measured before surgery and 24 hours after surgery. Investigators will record perioperative clinical information and postoperative neurological outcomes, including transient ischemic attack, stroke, delirium, and cognitive dysfunction. Approximately 90 participants are planned. The study will not assign any treatment or procedure.

Eligibility

Sex
ALL
Min age
35 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Age 35 to 90 years * Scheduled to undergo elective isolated carotid endarterectomy * Willing and able to provide informed consent and the required blood samples Exclusion Criteria: * Acute coronary syndrome within the previous 3 months * Carotid endarterectomy planned in combination with another surgical procedure * Atrial fibrillation * Known inflammatory disease * Hematologic disease * Refusal to provide preoperative consent or a blood sample * Stroke with residual neurological sequelae within the previous year * Multiple sclerosis, Alzheimer disease, Parkinson disease, or another pre-existing neurological disease

Primary outcome measure(s)

  • Number of Participants With Postoperative Neurological Complications — At hospital discharge
    Number of participants who experience at least one postoperative neurological complication after carotid endarterectomy: transient ischemic attack, stroke, delirium, or cognitive dysfunction. A participant with more than one event will be counted once in this composite outcome.

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences Bursa Yuksek Ihtisas Training and Research Hospital Bursa Bursa 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 NCT07843979 on ClinicalTrials.gov ↗ ← All trials in Turkey