Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06660602

Perioperative Cerebral Function Assessment for Cardiac Surgery

Led by China National Center for Cardiovascular Diseases · Updated on 2025-03-19

1845

Participants Needed

1

Research Sites

177 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Perioperative neurological complications in cardiovascular surgical procedures are associated with a significant risk of mortality and disability. This study is aimed at identifying the specific risk factors associated with these neurological complications during the perioperation and developing a comprehensive predictive model designed to enhance clinical decision-making and improve patient safety. The research is divided into three key phases: preoperative, intraoperative, and postoperative, each involving targeted evaluations and continuous monitoring to provide a thorough assessment of patient risk and outcomes.

CONDITIONS

Official Title

Perioperative Cerebral Function Assessment for Cardiac Surgery

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-80 years
  • Patients undergoing cardiovascular surgical procedures
  • Able to understand and comply with the clinical trial protocol requirements, and willing to sign the informed consent form.
Not Eligible

You will not qualify if you...

  • Unable to tolerate required diagnostic procedures such as neck CT angiography, head CT perfusion, or electroencephalography due to physical limitations or medical reasons
  • Severe renal insufficiency with creatinine clearance less than 30 mL/min or serum creatinine more than twice the upper limit of normal
  • Severe liver dysfunction including ALT or AST greater than three times the upper limit of normal, acute or chronic hepatitis, cirrhosis, or other significant liver diseases
  • Comorbid conditions that may compromise study participation or pose substantial risk, including alcohol or substance abuse, malignancies, and severe diseases affecting liver, kidneys, lungs, endocrine system, or hematopoietic system
  • Inability to cooperate with study procedures due to cognitive, psychological, or physical factors
  • Other conditions deemed unsuitable by the investigator for safe or effective participation

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

Department of Neurology, Fuwai Hospital, Chinese Academy of Medical Sciences

Beijing, China

Actively Recruiting

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Research Team

Y

Yao Feng, Dr.

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

0

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