Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07561970

COmparison of Maintenance of Propofol And Sevoflurane Spectral Study

Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2026-05-01

280

Participants Needed

1

Research Sites

85 weeks

Total Duration

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AI-Summary

What this Trial Is About

Lower EEG alpha band power is currently extensively studied as a potential biomarker of brain vulnerability. No previous study has evaluated whether there was a difference in EEG power spectrum ranges between propofol and sevoflurane, the two main anesthetic agents for maintenance of general anesthesia, in order to define a cut-off value for the prediction of a higher risk of postoperative delirium. * Primary objective: comparison of EEG alpha power (dB) during maintenance of anesthesia with propofol and sevoflurane using data available in the NeuroSense® depth-of-anesthesia monitoring * Secondary objectives: comparison of other EEG frequency bands during maintenance of anesthesia with propofol and sevoflurane using data from the NeuroSense® depth-of-anesthesia monitoring

CONDITIONS

Official Title

COmparison of Maintenance of Propofol And Sevoflurane Spectral Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients undergoing elective electrophysiological interventions, such as atrial fibrillation ablation procedures, under general anesthesia
  • Able to give informed consent
  • French-speaking patients
Not Eligible

You will not qualify if you...

  • Need for premedication with benzodiazepine before anesthesia
  • Reduced left ventricular ejection fraction (< 50%) or cardiac conditions requiring balanced anesthesia with benzodiazepine and/or ketamine
  • Preoperative MoCA score below 26/30 for patients aged 55 years or older
  • Treatment with anti-epileptic drugs
  • Treatment with benzodiazepines for anxiety or sleep disorders
  • Emergency procedures
  • Morbid obesity with BMI over 40 kg/m2
  • History of severe postoperative nausea or vomiting

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

Cliniques universitaires Saint-Luc

Brussels, Belgium, 1200

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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