Improving sedation practices for critically ill patients on mechanical ventilation

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 initiative aims to enhance sedation practices for patients in intensive care units (ICUs) who require mechanical ventilation. By utilizing neurophysiological and respiratory targets, the study seeks to optimize sedation levels, reducing the risks associated with oversedation and improving patient comfort. The approach involves a collaborative effort among healthcare providers at Oslo University Hospital to establish a more objective and effective sedation strategy. The goal is to minimize variability in sedation practices and improve overall patient outcomes in critical care settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Admitted to ICU
* Estimated need for sedation \> 24 hours

Exclusion Criteria:

* Patients admitted for palliative care
* Patients admitted with restrictions in care (no ventilator treatment)
* Contraindication for daily interruption of sedation

Where it's running

• Oslo University Hospital
  Oslo, Oslo, Norway Recruiting

Study contacts

• Study coordinator: Theresa M Olasveengen, MD PhD
• Email: uxothe@ous-hf.no
• Phone: +4741419930

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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.