Clinical Trials Directory

Trials / Terminated

TerminatedNCT04246892

Impact of Alarm Reduction on Delirium in ICU

Status
Terminated
Phase
Study type
Observational
Enrollment
89 (actual)
Sponsor
Central Hospital, Nancy, France · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

Delirium is an acute and fluctuating disturbance of consciousness and can occur in 80% of critically ill patients. Delirium is more frequent in mecanically ventilated patients and is associated with longer hospital stay, increased cognitive impairment and mortality. On the occasion of the change of the monitors in the ICU ward, allowing a total withdrawal of alarms in patients room, this study evaluates the prevalence of delirium before and after the alarm withdrawal. During the first period the patients will be monitored as usual, and during the second period patients will be monitored without alarms ringing in patients room. Delirium will be screened with a validated, clinical tool.

Conditions

Timeline

Start date
2020-02-03
Primary completion
2023-02-23
Completion
2023-02-23
First posted
2020-01-29
Last updated
2023-08-30

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04246892. Inclusion in this directory is not an endorsement.

Impact of Alarm Reduction on Delirium in ICU (NCT04246892) · Clinical Trials Directory