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Neuroprotection for children with anesthsia: influencing factors for Emergence Delirium

Neuroprotection for children with anesthsia: influencing factors for Emergence Delirium

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00020246
Enrollment
150
Registered
2019-12-10
Start date
2019-12-13
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F05.8

Interventions

Group 1: A processed EEG is registered while the children are under anesthesia. After anesthesia a score is evaluated to detect Emergence Delirium.

Sponsors

Klinik für Anästhesiologie und operative Intensivmedizin, Katholisches Klinikum Bochum.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 6 Years

Inclusion criteria

Inclusion criteria: Children Age 0-6 years, who recieve ENT-surrgery in the St. Elisabeth-Hospital in Bochum (Germany), ASA I-II

Exclusion criteria

Exclusion criteria: premature birth (< 32 gestational week), contraindication against standard anesthetics, neurological disease

Design outcomes

Primary

MeasureTime frame
Incidence of Emergence Delirium

Secondary

MeasureTime frame
blood pressure, heart rate, end tidal carbon dioxide concentration, peripheral oxygen Saturation, lab result, Wilton score to assess sedation depth, routinely assessed pain scores with CHIPPS or FACES Pain Scale, EEG assessment, ASA score

Countries

Germany

Contacts

Public ContactPhilipp Gude

Klinik für Anästhesiologie und operative Intensivmedizin, Katholisches Klinikum Bochum.

p.gude@klinikum-bochum.de0234-509-3211

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026