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Impact of Alarm Reduction on Delirium in ICU (ALADIN)

C

Central Hospital, Nancy, France

Status

Terminated

Conditions

Delirium

Study type

Observational

Funder types

Other

Identifiers

NCT04246892
2019PI225

Details and patient eligibility

About

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.

Enrollment

89 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age>18 years, admission to ICU

Exclusion criteria

  • length of stay in ICU<24 hours, moribund patient, deafness, dementia, psychiatric pathology, delirium at admission, acute neurological pathology at admission (stroke, epilepsy, neuro-infection), hepatic encephalopathy, admission for cardiac arrest, admission for voluntary drug intoxication, pregnancy

Trial design

89 participants in 2 patient groups

group before alarm withdrawal
groupe after alarm withdrawal

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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