Clinical trial Recruiting at 1 site Observational Ages 60 and up

Assessing cognitive and neurophysiological outcomes after open heart surgery

Official title: Postoperative Clinical and Neurophysiological Assessment of Patients After Open Heart Surgery

Run by Ain Shams University · NCT06707454 · Data updated 2026-11-12

This study looks at how open heart surgery affects thinking and brain function in patients, using special tests to see if their brain activity before surgery can predict how well they will think afterward.

Quick facts

Study typeObservational
Ages60 Years and up
SexAll
Enrollment80 (estimated)
SponsorAin Shams University
Academic / other
Locations1 site (Cairo)
StatusRecruiting
StartedJune 1, 2023
Main results expectedMay 1, 2025
Study endsMay 1, 2025
Registry record updatedNovember 27, 2024
Trial IDNCT06707454 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients aged 60 and older scheduled for on-pump open heart surgery, either isolated CABG or combined CABG and valve surgery.

Probably not a fit

Patients with a history of central nervous system diseases, severe cognitive impairment, or those unable to undergo DEEG recordings may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the clinical, cognitive, and neurophysiological outcomes of patients who have undergone open heart surgery, specifically focusing on those undergoing coronary artery bypass grafting (CABG). It utilizes digital electroencephalography (DEEG) to assess preoperative neurophysiological status and its correlation with postoperative cognitive function. The study aims to gather data from a sample of Egyptian patients to better understand the impact of cardiac surgery on cognitive health. The findings could help in predicting cognitive outcomes based on preoperative assessments.

Why it matters

Potential benefit: If successful, this study could enhance postoperative care by identifying patients at risk for cognitive decline after heart surgery.

How similar studies have gone: Other studies have shown success in using neurophysiological assessments to predict cognitive outcomes after cardiac surgery, indicating that this approach is supported by existing research.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient ≥ 60 years.
* Both sexes.
* Patients who are scheduled for on-pump open heart surgery either isolated coronary artery bypass grafting (CABG) or combined CABG and valve surgery.

Exclusion Criteria:

* Patients with a past history of CNS disease (e.g. Epilepsy, brain tumors, or Dementia).
* Patients with metabolic disturbance.
* Illiterate patient.
* Patient with sever cognitive impairment on Mini-mental state Examination (MMSE) and/or Montreal Cognitive Assessment (MoCA)
* Patients who cannot undergo DEEG recordings (eg, uncooperative).
* Patients with abnormal brain images except for small vessel disease.

Where it's running

  • Ain Shams University
    Cairo, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.