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Prevention of Delirium With Light in the Intensive Care Unit — PreDeLight-ICU  

Delirium Clinical Trial

Official title:
Prevention of Delirium With Light in the Intensive Care Unit

Clinical Trial Summary

The purpose of this multicenter randomised controlled trial is to investigate if circadian light at the patients bedside (using Philips HealWell system, CE marked)significantly reduces prevalence of delirium in mechanically ventilated intensive care unit patients.

Clinical Trial Description

Patients, who are randomly assigned to the "Lightening arm" will have the circadian light for the whole ICU stay. Light levels at the patients bedside will be measured continuously: embedded light sensors provide irradiance and luminous lux recordings in red, green, and blue color bands and a white light measurement in lux ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01727375
Study type Interventional
Source Charite University, Berlin, Germany
Contact
Status Withdrawn
Phase N/A
Start date July 2013
Completion date November 2016
View Details
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