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Recruiting NCT06692309

Exploring the Predictive Value of Electroencephalography Features in Perioperative Neurocognitive Disorders Following Cardiovascular Surgery

Observational Cardiovascular Surgery Perioperative Neurocognitive Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: cardiovascular surgery.
Who it may be relevant to
Registry conditions: Cardiovascular Surgery, Perioperative Neurocognitive Disorders. Basic parameters: from 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

To Explore the Predictive Value of Electroencephalography Features in Perioperative Neurocognitive Disorders in Patients Undergoing Cardiovascular Surgery Under General Anaesthesia: a Single-centre Prospective Observational Study

Overview

To explore the predictive value of Electroencephalography features in Perioperative Neurocognitive Disorders in patients undergoing cardiovascular surgery under general anesthesia

Detailed description

Data was acquired on the ward using a 10-20 system with a standard 32-channel EEG cap and an EEG instrument (BP Company, Gilching, Germany). Patients were tested using cognitive assessment scales before and after surgery.

Cognitive levels were assessed 1 day before surgery and 1 week after surgery (7±2 days) using the Montreal Cognitive Assessment (MoCA) . Patients were followed up one month (30±2 days) after surgery using the Telephone version of the Montreal Cognitive Assessment Scale (T-MoCA).

Preoperative and postoperative electroencephalography brain network-related indexes (such as cluster coefficient, small world index, etc.) in patients with PND will be included in the analysis.

Interventions

  • Procedure cardiovascular surgery
    Heart bypass surgery; Heart valve replacement surgery

Primary outcome measures

  • The predictive value of preoperative Electroencephalography features in patients with postoperative cognitive dysfunction following cardiovascular surgery [Time frame: 2025.08]
Secondary outcome measures (2)
  • The predictive value of preoperative Electroencephalography features in patients with postoperative delirium following cardiovascular surgery [Time frame: 2025.08]
  • Electroencephalography features in patients with postoperative delirium [Time frame: 2025.08]

Eligibility criteria

Inclusion criteria

  • Written informed consent
  • undergoing coronary artery bypass surgery or valve replacement surgery under general anaesthesia
  • ASA grade: II-IV
  • older than 60 years
  • Able to complete cognitive function tests

Exclusion criteria

  • history of severe neurological diseases and psychiatric diseases
  • history of drug abuse
  • severe hearing or vision impairment
  • preoperative delirium
  • serious adverse reactions such as cardiac arrest and cardiopulmonary resuscitation during surgery
  • patients undergoing secondary surgery in a short period
  • participation in concurrent clinical trials

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

China · 1 center
  • Beijing Chao Yang Hospital — Beijing

Identifiers

NCT: NCT06692309 · DXK2022-ke-487

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗