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Adequate Depth of Anesthesia: the Anesthesiologist's Assessment and the EEG Processed Monitoring

K

Kepler University Hospital

Status

Completed

Conditions

Anesthesia

Treatments

Device: EEG monitoring

Study type

Observational

Funder types

Other

Identifiers

NCT02766894
C-109-16

Details and patient eligibility

About

Comparison of conventional assessment of anesthetic depth by anesthesiologists (moderate, deep or light anesthesia) with EEG monitoring (Narcotrend® state/index). In case of mismatch statistical analysis for underlying factors are done.

Full description

In this observational study estimation of anesthetic depth by anesthesiologists is compared with the EEG based monitoring Narcotrend®. 10-20 voluntary anesthesiologists of the Kepler University Hospital, unfamiliar with EEG-monitoring during anesthesia, assess depth of anesthesia (moderate, deep or light level) during a steady-state period by clinical signs and measured or calculated concentrations of anesthetics. Concurrently Narcotrend® provides data of anesthetic depth (index, stadium) blinded for the anesthesiologist. Each anesthesiologist is included 30 times during study period. The aim of this study is to define conformity between subjective and objective assessment of narcotic depth. In the cases of divergence data of the patient (age, body mass index, comorbidity...), data of the anesthesiologist (age, years of practice...), data of anesthesia (balanced anesthesia, target controlled infusion, endtidal concentration of volatile anesthetic...) and data of the operation (eye surgery, cardiac surgery...) will be analyzed by statistics with regard to underlying or concomitant factors. These findings could help to develop recommendations in the use of EEG-processed monitoring to improve subjective assessment and facilitate an adequate depth of anesthesia to be provided for every patient.

Enrollment

600 patients

Sex

All

Ages

1 to 110 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • operation under general anesthesia
  • duration of surgery ≥ 10 minutes
  • informed consent
  • ASA physical status 1-4
  • age 1-110y
  • performance check of Narcotrend

Exclusion criteria

  • proximity of EEG electrodes to the operating field
  • frontal skin lesion
  • frontal cerebral pathology
  • hypoxic brain damage
  • hypothermia (≤33°C)
  • language barrier

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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