Understanding delirium in adult and pediatric ICU patients in the Czech Republic

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to investigate the incidence and management of delirium in adult and pediatric patients admitted to intensive care units in the Czech Republic. It will follow two cohorts: adults with acute strokes in neurocritical care and children aged 6-18 years in pediatric intensive care. The study will assess the effectiveness of current delirium screening and prevention strategies over a minimum follow-up period of six months. By identifying gaps in knowledge and implementation of delirium management recommendations, the study seeks to improve patient outcomes in critical care settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Neurointensive/neurocritical group (N-ICU): patients with acute ischaemic or haemorrhagic stroke admitted to the Stroke Unit or ICU of the Department of Neurology, University Hospital Brno (NK-UHB).
* Paediatric intensive/critical group (P-ICU): children aged 6-18 years, admitted to the Paediatric ICU - Department of Paediatric Anaesthesiology and Intensive Care (KDAR-UHB) with a stay of at least 24 hours (including postoperative care).

Exclusion Criteria:

* (N-ICU) severe trauma with short life expectancy (days)
* duration of the ICU stay shorter than 24 hours

Where it's running

• Brno University Hospital
  Brno, Czechia Recruiting

Study contacts

• Study coordinator: Josef Bednařík, prof. MD, CSc.
• Email: bednarik.josef@fnbrno.cz
• Phone: 532231481

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.