Validation of a Processed EEG Device for Monitoring Sedation in PICU

Recruiting Observational Study
Sedation Complication
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
1 Day – 18
Sex
Female
Study type
Observational
Participants needed
150 (estimated)
Sponsor
Azienda Ospedaliera di Padova · Other
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About This Trial
The goal of this prospective observational study is to validate pEEG as a monitoring tool for the analgosedation level in mechanically-ventilated critically ill children, receiving or not-receiving NMBAs. The main question aims to answer is to measure the strength of agreement between pEEG score and Comfort Behavioural Scale (CBS) (goal standard). Participants will be monitored with pEEG and CBS …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: \- sedated and ventilated patients admitted in PICU Exclusion Criteria: * skin lesions * significant traumatic lesions in the area where the Masimo Sedline® sensor need to be applied.
Contacts

angela amigoni, MD

+39 339 8333765

angela.amigoni@aopd.veneto.it

CONTACT

anna tessari

+ 39 3497804876

anna.tessari@aopd.veneto.it

CONTACT