Actively Recruiting

Age: 18Years - 70Years
All Genders
NCT07000461

Transcranial Doppler as a Predictor of Postoperative Cognitive Dysfunction Following Cardiopulmonary Bypass

Led by Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Updated on 2026-02-17

106

Participants Needed

1

Research Sites

54 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Neurological dysfunction either transient or permanent is a major cause of morbidity and mortality after cardiopulmonary bypass, and cognitive dysfunction is more frequent in cardiac surgery than in non-cardiac procedures. Variations in cerebral blood flow and oxygen extraction are considered key contributing factors. Although pulsatile flow during bypass has shown benefits for renal function and recovery, its effects on postoperative neurological dysfunction and delirium remain unclear due to limited research. This study aims to evaluate the impact of pulsatile versus non-pulsatile cardiopulmonary bypass flow on POCD in adult CABG patients by measuring middle cerebral artery (MCA) flow using transcranial Doppler.

CONDITIONS

Official Title

Transcranial Doppler as a Predictor of Postoperative Cognitive Dysfunction Following Cardiopulmonary Bypass

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-70
  • Scheduled for isolated elective cardiopulmonary bypass surgery
Not Eligible

You will not qualify if you...

  • Carotid stenosis 50% or greater
  • Emergency patients or those with a history of reoperation
  • History of cerebrovascular events
  • Patients who do not provide consent
  • Temporal window failure
  • Ejection fraction below 40%
  • Mini-Mental State Examination score below 23
  • Mechanical ventilation for more than 24 hours or reintubation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Sema Nur Baki, M.D

CONTACT

D

Dicle Birtane, M.D, FCCM

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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