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NCT04841122

Improved Patient Safety for Acute Restless Medical Patients With Supplemental Observation

Terminated NA Last updated 1 November 2021
What this trial tests

NA trial testing Camera observation in Delirium in 8 participants. Terminated before completion.

Timeline
19 April 2021
Primary endpoint
30 September 2021
30 September 2021

Quick facts

Lead sponsorAalborg University Hospital
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingsingle
Primary purposesupportive care
Enrollment8
Start date19 April 2021
Primary completion30 September 2021
Estimated completion30 September 2021
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Aalborg University Hospital

Who can join

Adults 65 to 100, any sex, with Delirium. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to investigate whether supplemental camera observation directly linked to the nurse's phone will improve patient safety for acute medical care patients', who are restless, confused or in risk of development of acute delirium. The setting is an acute medical care ward. The expected result is a reduced incidence of patients with delirious condition, patients who fall or unintentionally remove intravenous access or catheters. Thus, higher patient safety and more efficient patient trajectories are expected, as well as a reduced need for treatment, care and rehabilitation after discharge.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Delirium

Currently open trials in the same condition.

Other Aalborg University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04841122.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing